Money & recalls you may be owed
Browse current Canadian class-action settlements and product & vehicle recalls. Check the deadline, then go straight to the official administrator.
246 listing(s)
El Mexicano brand Agua Fresca de Horchata Instant Horchata Drink recalled due to improperly declared milk
El Mexicano brand Agua Fresca de Horchata Instant Horchata Drink recalled due to improperly declared milk.
Nature's Best Organic Peanut Butter
Potential Salmonella contamination.
Les Fermes Lufa brand Broccoli microgreens recalled due to pathogenic E. coli
The affected product is being recalled from the marketplace due to possible pathogenic E. coli contamination.
Philips Allura Xper Systems
Under certain conditions, the hand switch button may not fully release after being pressed, potentially resulting in loss of imaging functionality or unintended radiation exposure and potentially additional contrast medium injection.
Giraffe™ OmniBed™ Carestation™
GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury.
Harmony™ Delivery Catheter System
Medtronic had received two (2) complaints about Harmony™ DCS distal tip detachment during the implant procedure. A root cause investigation has identified that, due to a manufacturing issue, Harmony™ DCS from specific manufacturing lots may have an increased potential for distal tip detachment under certain procedural or anatomical conditions.
Renpure Tea Tree & Rosemary Scalp Rebalancing Shampoo & Conditioner recalled due to microbial contamination
These lot codes have elevated microbial levels including aerobic bacteria count, yeast/mold count and Burkholderia cepacia complex which may cause irritation and sensitivity to the user. People with certain health problems including weakened immune systems or chronic lung disease may be more susceptible to infections from B. cepacia. Yeast can cause fungal infections in individuals whose skin and/or immune system is compromised. As of June 3, 2026, the company has received no reports of incident or injury in Canada.
Cosyland Kids Kitchen Step Stools recalled due to fall and entrapment hazards
The recalled Kids Kitchen Step Stools can collapse or tip over while in use, and a child’s torso can fit through the openings on the front and back sides, posing a risk of serious injury and death due to tip over, fall and entrapment hazards. As of June 1, 2026, the company has received no reports of incident or injury in Canada. In the United States, the company has received 25 reports of incidents involving stability issues and falls and 8 reports of injuries ranging from scrapes and contusions to a fractured arm.
Safrax ODOR-CLO2 Chlorine Dioxide Odor Removal- Air Freshener & Deodorizer recalled due to improper labelling and lack of child-resistant packaging
The recalled product does not meet the labelling and child-resistant packaging requirements of the Consumer Chemicals and Containers Regulations, 2001 under the Canada Consumer Product Safety Act. The lack of appropriate labelling information and child-resistant packaging could result in unintentional exposure to the product and lead to serious illness or injury including death. As of June 2, 2026, the company has received no reports of incident or injury in Canada.
Tako Wasabi products recalled due to undeclared fish
The affected products are being recalled from the marketplace because they contain fish which is not declared on the label.
PMS-Fluconazole 50 mg tablets; Incorrect quantity of tablets
The affected batch may not contain the correct quantity of tablets.
Baxter Corporation products recall; Blue cap breakage
Blue Caps Enhanced Closures (blue tip protectors) may break apart in affected lots.
Allo simonne brand Milk Chocolate Spread recalled due to pieces of glass
Allo simonne brand Milk Chocolate Spread recalled due to pieces of glass.
Urban Shades Roller Shades recalled due to strangulation hazard
Health Canada has determined that the recalled window coverings do not meet the Corded Window Coverings Regulations and pose a strangulation hazard. Young children may pull looped cords around their neck, or become entangled in the cords, causing a strangulation hazard. Health Canada recommends cordless window coverings. For more information on the hazard, see Blind Cord Safety. As of June 5, 2026, the company has received no reports of incident or injury in Canada.
Wiifo Children’s Tower Stools recalled due to fall and entrapment hazards
The recalled tower stools can collapse or tip over while in use, and a child’s torso can fit through the openings on the tower’s sides, posing a risk of serious injury and death due to tip over, fall and entrapment hazards. As of June 1, 2026, the company has received no reports of incident or injury in Canada.
Expanded recall: Nightgowns with various prints recalled due to flammability hazard
The recalled nightgowns violate the flammability requirements for children’s sleepwear, posing a risk of burn injuries to children. Loose-fitting children’s sleepwear can contact ignition sources such as stove elements, candles, and matches more readily than tight-fitting sleepwear, and once ignited will burn rapidly, potentially resulting in severe burns to large areas of the child’s body. As of June 3, 2026, the company has received no reports of incident or injuries in Canada.
Guedel Airway
During manufacture, some devices have been identified with occluded or partially occluded tips of the Guedel Airway.
Health Canada warns that COHEALI Wooden Pacifier Clip for baby previously available on Amazon.ca may pose a risk of choking
The product is intended for children under three years of age. The screw linking the wooden piece to the metal clip can become loose posing a choking risk to children.
CannaPiece Corp. recalls Wild West 96+ Strawberry Stampede Liquid Diamonds 510 Vape due to a labelling issue
The label for the affected product has incorrect cannabinoid values. The label shows that the THC is lower than the actual value.Without knowing the accurate THC level in the product, it could be difficult to make informed decisions regarding your cannabis use. This may lead to over-intoxication and temporary adverse health consequences associated with THC overdose, which could include:confusiondisorganized thinkingphysical and mental impairmentanxietyfear or panicdecreased blood pressureelevated heart rateIn remote cases, depending on the individual and the dose of THC consumed, THC overdose can also result in psychotic episodes characterized by paranoia, delusion or hallucinations. These effects could in some cases lead to an emergency department visit or hospitalization.
Selenia Dimensions 2D/3D Mammography Systems
Hologic is initiating this voluntary field safety corrective action because the vertical travel assembly on 3Dimensions and Selenia Dimensions systems may experience internal bolt failure over time. The vertical travel assembly contains eight internal bolts that secure the c-arm to the assembly. Devices with loose, missing or broken bolts may exhibit shaking, vibration or uncommanded c-arm motion.
Nicotine Pouch Recall; No market authorization
Product sold without market authorization (DIN) in Canada.
Tip Restraint Kits included in Childcraft Furniture recalled due to tip-over and entrapment hazards to children
The recalled plastic tip restraint kits (also referred to as furniture straps) can break or degrade, posing tip-over and entrapment hazards that can result in serious injuries or death to children or elderly consumers interacting with furniture that is secured to the wall with the defective plastic tip restraints. This is a hidden defect because consumers who purchase and install this product may be under a false sense of security that their furniture is safe from a tip-over incident.As of June 1, 2026, the company has received no reports of incident or injury in Canada. In the United States, there have been no reports of incident or injury.
ETMS 70 mm Cooled Coil
A potential issue manifests as an electrical arc within the coil itself that, when occurs, leads to a relatively loud popping sound, which can startle the patient or operator.
Aptima HIV Quant Dx Assay, HCV Quant Dx Assay, and HBV Quant Assay Software
This notification is to inform Panther and Panther Fusion users that assay installer (version 2.0.0.9) including the Aptima HIV Quant Dx Assay, HCV Quant Dx Assay, and HBV Quant Assay software was installed on Panther and Panther Fusion systems prior to Health Canada approval.The Aptima HIV Quant Dx Assay, HCV Quant Dx Assay, and HBV Quant Assay software included in assay installer version 2.0.0.9 have not been approved by Health Canada but have been validated and released. Based on this, the configuration does not affect assay performance, compromise the accuracy of test results, or impact product performance.
Lactantia brand UltraPūr 2% M.F. Lactose Free Dairy Product recalled due to over-fortification of Vitamins A and D
The affected product is being recalled from the marketplace due to over-fortification of Vitamins A and D.
Lancora Tablets; Broken / partial tablets in blister pack
Presence of partial tablets in the blister packs.
Unauthorized soft-shelled hyperbaric chambers may pose serious health risks 2026-06-16
Health Canada has received several complaints related to the use of unauthorized soft-shelled hyperbaric chambers and they are increasingly found in wellness centres in Canada. Soft-shelled hyperbaric chambers are regulated as medical devices under the Food and Drugs Act and Medical Devices Regulations. These devices are unlicensed, may be ineffective for the purposes for which they are advertised and may pose serious health risks for users and those in close proximity, including death.Soft-shelled hyperbaric chambers may catch fire, especially when used in combination with an oxygen concentration device. They can suffocate users, spread infectious diseases between users, cause damage to ears, eyes, sinuses, lungs and teeth, and change blood sugar levels.To date, Health Canada has not authorized any soft-shelled hyperbaric chamber for sale in Canada, as it has not received the evidence needed to confirm that these devices meet Health Canada's safety, effectiveness or quality requirements. As a result, it is illegal to import, sell and advertise soft-shelled hyperbaric chambers in Canada.Do not confuse soft-shell hyperbaric chambers with hard-shell hyperbaric chambers. Hard-shell devices are proven to treat 14 specific conditions. You can learn more about hard-shell hyperbaric chambers on Health Canada's website.The Department is following up on complaints and will take compliance and enforcement actions, as needed, to mitigate the risk to Canadians using the most appropriate level of intervention, in accordance with its Compliance and enforcement policy for health products.
GE Healthcare Integrated and Stand-Alone Resuscitation systems
GE HealthCare has become aware of a potential issue involving the air-oxygen blender knob shaft on certain (serial number specific) integrated and stand-alone Resuscitation systems. In some cases, the blender knob shaft can loosen, which can affect the delivered oxygen concentration. If this occurs, the system can deliver an oxygen concentration that does not match the intended concentration set by the user, potentially resulting in hypoxia or hyperoxia in the patient.
Ernest Cider brand Sangria Cider recalled due to yeast
Ernest Cider brand Sangria Cider recalled due to yeast.
Expanded recall: U Kids We Love Cozy 2-piece Pajamas Sets and Lounge Pants recalled due to flammability Hazard
The recalled 2-piece pajama sets and lounge pants violate the flammability requirements for children’s sleepwear, posing a risk of burn injuries to children.Loose-fitting children’s sleepwear can contact ignition sources such as stove elements, candles, and matches more readily than tight-fitting sleepwear, and once ignited will burn rapidly, potentially resulting in severe burns to large areas of the child’s body.As of June 12, 2026, the company has received no reports of incident or injuries in Canada.
Single Use Distal Cover
Olympus has developed a newly designed version of the MAJ-2315 to help mitigate the risk of incorrect attachment of the distal cover to the scope. Users should stop using the old design and set aside for return once the new design of the MAJ- 2315 has been received.
Plum™ Precision IV Pumps
In a specific scenario, the pump will not decrement the Volume to be Infused (VTBI) displayed on the Delivery screen and may deliver up to twice the VTBI at the programmed rate.
Polyflex powder for suspension; Cracked vials
Glass vials may be cracked in the affected lots.
Joolz Aer2 Car Seat Adapter Set recalled due to fall hazard
The Joolz Aer2 Car Seat Adapter may fail to properly attach to the Aer2 stroller chassis, which may allow the car seat to fall.As of June 3, 2026, the company has received no reports of incident or injury in Canada. In the United States, the company has received one report of incident and no injuries. The company is aware of 28 reports of incidents and two reports of injuries globally.
Arizer Solo III Intergalactic (Black) Portable Vaporizers recalled due to fire and burn hazards
The internal lithium-ion battery can ignite or explode, posing fire and burn hazards.As of June 2, 2026, the company has received no reports of incidents or injuries in Canada. In the United States, the company has received four reports of incidents and no reports of injuries.
MED-RX Wound Care Kit
CHS was notified by BD Canada that they are conducting a recall of specific lots of the BD Chloraprep™ Clear - 1 ml and Clear 1.5 ml applicators. The BD Chloraprep™ Clear - 1 ml and Clear 1.5 ml applicators with paper lidding are being recalled due to potential breach of sterility in the packaging, due to wrinkles in the paper lidding which may extend to the seal area.CHS Ltd uses these Chloraprep applicators in the medical devices they manufacture.
Atellica CH Enzymatic Hemoglobin A1c (A1c_E) assay
Siemens Healthineers has confirmed, through internal investigation of customer complaints, the potential for intermittent well-to-well bias affecting the A1c_E/A1c_H assay when used on the Atellica CH and Atellica CI systems. This observed bias does not affect every A1c_E reagent lot or reagent pack. However, affected wells cannot currently be identified prospectively, therefore all in-date lots are considered potentially impacted until further notice. Under certain circumstances, this issue may result in:. Falsely depressed patient results when lot calibration is performed using an affected well and patient testing is subsequently performed using an unaffected well.. Falsely elevated patient results when lot calibration is performed using an unaffected well and patient testing is subsequently performed using an affected well.
Wu Xian Zhai brand Soybean Snacks recalled due to undeclared wheat and / or egg
The affected products are being recalled from the marketplace because they contain wheat and / or eggs which are not declared on the label.
BD MaxPlus ™ Connector Minibore Extension Set
BD has identified a mechanical issue with internal sterilization equipment resulting in potential under dosing of product during processing, which may have resulted in product not being sterilized correctly.
FARADRIVE™ Steerable Sheath
Boston Scientific is communicating to customers of a forthcoming update to the FARADRIVE™ Steerable Sheath Instructions for Use (IFU).Air embolism is a known procedural risk associated with left atrial ablation procedures utilizing transseptal sheaths and catheter exchanges and is addressed within the device labeling. Boston Scientific continuously monitors product performance and customer feedback as part of its quality system and ongoing product improvement activities. Ongoing product performance monitoring confirms that the FARADRIVE sheath continues to perform within established design, safety, and anticipated product performance expectations. The observed rate of air embolism events remains very low at 0.0134%, consistent with the air embolism incidence of less than 1% reported.
Portable Hook-On Chair recalled due to fall hazard
The recalled portable hook-on chair poses a fall hazard because the crotch restraint can be removed without the use of a tool and infants can fall through an opening, posing a fall hazard.As of June 12, 2026, the company has received no reports of incident or injury in Canada.
CyberKnife® Treatment Delivery System
During collimator housing drop-off or pickup over the Xchange® table, the system may interlock, stop motion, and prompt service contact. Remove the patient before troubleshooting, do not move the treatment robot using the in-room pendant, and contact accuray service.
Penumbra System RED 68 Reperfusion Catheter
Penumbra has identified an issue in the lots of RED 68 specified in this notification which may result in potential fracture of the device. Penumbra has not received reports of any events involving patient injury related to these fractures; however, fracture of the catheter may result in patient injury or death.
Gyrus ACMI® Classic Series Continuous Flow Resectoscope
This recall action is being taken because it has been determined that some of the sets of sterilization parameters provided in the IFU may not consistently render the devices adequately sterile.
A.T.S® 4000 TS Tourniquet Systems Single and Dual Hose with CPC Connectors
Zimmer Biomet is conducting a medical device recall for A.T.S® 4000 TS Tourniquet Systems Single and Dual Hose with CPC Connectors. One (1) complaint was received with no clinical impact reporting that wrinkles were identified in the sealing area of the sterile pouch. Subsequent seal integrity testing conducted internally showed potential sterility breach in 0.92% of inspected units that had visual seal nonconformities. The devices are distributed in cases (CS) of 20 units. Inside each case are two boxes (BX) of 10 units each.
Hoffmann® II Carbon Connecting Rod
Subsequent to product complaints, Stryker has confirmed that cracking of the Hoffmann® II Carbon Connecting Rods may occur following cleaning and sterilization.
Optima XR240amx X-Ray System
Mobile X-ray column assembly issue on certain Optima XR200/220/240amx systems.
Izem Energy brand Energy by ifri recalled due to labelling issues
Izem Energy brand Energy by ifri recalled due to labelling issues.
Infinion™ CX Contact Lead Kit
Boston Scientific is initiating a voluntary removal of unused Infinion™ CX Leads as part of the planned transition to the next generation lead (Infinion Pro). this action does not affect the devices that have already been implanted. For leads already in use, continued routine follow-up is recommended.
UHI-4 High Flow Insufflation System - Insufflator
Olympus identified an increase in UHI-4 front-panel 'blackout' complaints, where the front-panel display turns off unexpectedly, and air delivery (insufflation) ceases. An Olympus field service representative will contact affected users to schedule a mutually convenient time to perform the offset adjustment.
Argon Medical Devices L-Cath™ PICC and Midline Catheters
Reports of leaking and/or cracking at the hub of the affected products. A cracked catheter hub on a PICC may compromise the integrity of the closed intravenous system
Baby Kithmas and Kids Kithmas Plaid Lounge Sets recalled due to flammability hazard
The recalled children’s sleepwear violate the flammability requirements for children’s sleepwear, posing a risk of burn injuries to children.Loose-fitting children’s sleepwear can contact ignition sources such as stove elements, candles, and matches more readily than tight-fitting sleepwear, and once ignited will burn rapidly, potentially resulting in severe burns to large areas of the child’s body.As of June 23, 2026, the company has received no reports of incidents or injuries in Canada or the United States.
Amana Through-the-Wall Air Conditioners or Heat Pumps recalled due to burn and fire hazard
The product does not comply with the electrical requirements in the applicable UL Standard. The heating element may be energized any time the unit is plugged in, regardless of the mode of the unit, and a ground fault in the equipment’s electric heater may pose a burn or fire hazard. As of March 27, 2026, the company has received no reports of incidents or injuries in Canada. In the United States, the company has received one report of plastic on the product melting and no reports of injuries.
Super Off-Road 12,000 mAh Solar Wireless Power Bank recalled due to fire hazard
The lithium-ion battery cell in the portable wireless charger may overheat and swell, posing a fire hazard.As of June 23, 2026, the company has received no reported incident and no reports of injury in Canada. In the United States, the company has received one report of two swollen batteries and no reports of injuries.
Spiriva Capsules ; Out-of-specification (uniformity of delivered dose)
The affected lot may not consistently provide the intended dose of medication with each use.
Various Salem Foods brand Ground Spices and Spice Blends recalled due to undeclared wheat, sesame and mustard
The affected products are being recalled from the marketplace because they may contain wheat, sesame and mustard which are not declared on the label.
Amy's brand Organic Lentil Soup (Less Sodium) recalled due to container integrity defects and spoilage
Amy's brand Organic Lentil Soup (Less Sodium) recalled due to container integrity defects and spoilage.
Remifentanil hydrochloride for injection; Out of specification (Assay & Impurity)
The assay and impurity is out of specification in the affected lots.
Certain Thermos Stainless King Food Jars and Sportsman Food & Beverage Bottles recalled due to Impact Injury and Laceration Hazards
If perishable food or beverages are stored in the container for an extended period of time, the stopper can forcefully eject when opened, posing serious impact injury and laceration hazards.As of June 24, 2026, the company has received 10 reports of incidents in Canada, and 3 reports of injuries.
Abiomed Introducer Kits with Impella Heart Pumps
Abiomed has initiated a voluntary medical device recall (correction) for all currently distributed Introducer kits that are used with Impella heart pumps to notify customers of a potential for unexpected introducer sheath leakage from the sidearm and under the sheath cap and along the hub score lines in the hub region. Introducer leakage may impair hemostasis and increase the risk of access-site bleeding, particularly in anticoagulated patients. This information is provided to support appropriate clinical awareness, monitoring, and patient support as needed. The identified defect does not affect any other packaged products within the pump set.
9227-8712 Québec Inc. brand and L'Érabeille brand Pure Maple Syrup recalled due to container integrity defects and spoilage
9227-8712 Québec Inc. brand and L'Érabeille brand and Pure Maple Syrup recalled due to container integrity defects and spoilage.
Wu Xian Zhai brand Vegetable Beef (Sauce) recalled due to undeclared wheat and egg
The affected product is being recalled from the marketplace because it contains wheat and egg which are not declared on the label.
Certain Five Star Shellfish Inc. brand oysters recalled due to Salmonella
The affected products are being recalled from the marketplace due to possible Salmonella contamination.
IPEX cement and primer products recalled due to improper labelling and lack of child-resistant packaging
The recalled products do not meet the labelling and child-resistant packaging requirements of the Consumer Chemicals and Containers Regulations, 2001 under the Canada Consumer Product Safety Act.The lack of appropriate labelling information and child-resistant packaging could result in unintentional exposure to the products and lead to serious illness or injury including death.As of June 25, 2026, the company has received no reports of incidents or injuries in Canada.
New Horse Riding Helmet 100 Fouganza recalled due to injury hazard
The strap passing in front of the ear can slide backwards, which could affect the optimal fit of the helmet on the head and create a hazard for the user.As of June 29, 2026, the company has received no reports of incident or injury in Canada.
LIFECODES LSA Class II
Werfen has identified that two beads within the LIFECODES LSA class II assay kit(s) may present different DQB1 specificities than previously understood:• Bead 42 / Antigen ID 242Previously associated with DQB1*02:01, this bead instead presents DQB1*02:02• Bead 44 / Antigen ID 244Previously associated with DQB1*02:02, this bead instead presents DQB1*02:01• Note: DQA1*02:01 is present on both beads and therefore not impacted.Due to this issue, certain reactivity patterns may appear differently than expected.
NephroMax High Pressure Nephrostomy Balloon Catheter
Boston Scientific is notifying you that the renal sheath for certain NephroMax™ high pressure nephrostomy balloon catheters may be packaged in a reversed orientation.Between November 2025 and April 2026, seven (7) complaints reported reversed sheath orientation upon opening. In all cases, the issue was identified and corrected prior to patient use. If the sheath orientation is not corrected prior to use, the non-tapered end may be inserted in the patient, which could increase resistance and result in difficulty advancing, withdrawing or positioning the catheter. The potential for patient harm is considered low because the issue is readily identifiable and can be corrected prior to use.
Fludeoxyglucose (18F) Injection; Cracket vial
Fludeoxyglucose (18F) vial containing 24.80 mL (30.23 GBq of the product) used to administered the drug to the patients was found to be broken at the bottom.
Combined Smoke, Combustible Gas & Carbon Monoxide Alarm recalled due to potential failure to operate
The Residential Detectors Regulations require that smoke detectors, heat actuated fire detectors and smoke alarms in Canada meet the applicable Canadian standards. The product does not have a Canadian certification mark and it is unknown if the alarm operates in the presence of smoke, posing a potential fire hazard.Health Canada reminds consumers that products that do not have a recognized Canadian certification mark may not meet Canadian performance standards and could fail or operate incorrectly. This could pose a risk to consumers who may not be alerted to a fire incident in their home. For more information on what to look for when purchasing a smoke alarm or detector, see Health Canada's Consumer Information - When purchasing smoke or carbon monoxide alarms, look for a Canadian certification mark.As of June 22nd, 2026, the company has not received reports of incidents or injuries in Canada.
Intramedullary Bone Saw Blade Assembly
Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Sawblade Assembly due to potential sterile barrier packaging damaged caused by the exposed saw blade. It was identified internally that the tip protector was incorrectly placed on the blunt end of the device instead of the sawblade, leaving the saw blade exposed. The exposed saw blade has potential to damage the sterile barrier pouch, which has potential to result in loss of sterility. There have been zero complaints received.
Urinary Catheter Trays containing Cliniclean Pericare Wipes
Based on customer feedback, BD has identified that the Cliniclean Pericare Wipes provided within urinary catheter trays may be potentially contaminated with a lubricant used during the manufacturing process.
Hybrid Hydrophilic Microguidewire
Performance variability affecting the hydrophilic coating of Hybrid007 guidewires in specific lots may increase friction during microcatheter navigation. This may require guidewire replacement to complete the procedure, potentially prolonging procedure time and increasing the risk of procedure-related complications.
Westside Sauce brand Bistro Honey Dill Sauce recalled due to undeclared mustard
Westside Sauce brand Bistro Honey Dill Sauce recalled due to undeclared mustard.
Vevor 4 in 1 Baby walker recalled due to physical hazard
Baby walkers have been banned in Canada since 2004.Children in baby walkers are exposed to hazards that would not normally be accessible if the child were not supported by the walker, posing a variety of risks of injury to the child. Children in baby walkers can also fall down the stairs, which could result in injury or death.As of June 26, 2026, the company has received no reports of incident or injury in Canada.
JAMP Chlorthalidone 12.5 mg tablet: Out of specification (Dissolution)
The dissolution may be out of specification in the affected lot.
Hotline IV Fluid Warmer System & Accessories
ICU Medical became aware of an increased likelihood of leakage in specific lots of L-70 Hotline Fluid Warming sets due to potentially inadequate solvent application at the tubing to return connector bond. Three (3) lots of L-70 Hotline Fluid Warming sets have an increased likelihood of leakage due to this issue.
Sunluway Oven Bottom Panel Replacement recalled due to burn hazard
During its operation, the protective coating of units experiences rapid thermal decomposition and scorching. This material defect exhibits severe paint cracking, large-scale peeling (delamination), and dense smoke generation (outgassing) inside the appliance.As of June 30, 2026, the company has received no reports of incidents or injuries in Canada.
TAVNEOS (avacopan) and Health Canada’s Review of Data Integrity Concerns
Health Canada is reviewing significant concerns regarding the data integrity of the pivotal ADVOCATE trial, which served as the primary efficacy study supporting the authorization of TAVNEOS (avacopan). AudienceHealthcare professionals involved in the treatment and management of patients with severe active anti-neutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis, including rheumatologists, nephrologists, pulmonologists, internal medicine physicians, family physicians, nurse practitioners, and pharmacists. Key messagesHealth Canada has identified significant concerns about the data that supported the authorization of TAVNEOS (avacopan). These concerns raise questions about the efficacy of TAVNEOS. Pending the outcome of Health Canada’s review of these concerns, healthcare professionals are advised to:NOT initiate treatment with TAVNEOS in new patients.Contact and monitor patients currently receiving TAVNEOS and assess whether continued treatment remains appropriate. Background InformationTAVNEOS (avacopan) is indicated for the adjunctive treatment of adult patients with severe active anti-neutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis (granulomatosis with polyangiitis [GPA] and microscopic polyangiitis [MPA]) in combination with standard background therapy including glucocorticoids. TAVNEOS is not indicated for use as monotherapy and does not eliminate glucocorticoid use.The authorization of TAVNEOS in Canada (April 2022) was supported primarily by the pivotal Phase 3 ADVOCATE trial, sponsored by ChemoCentryx, which evaluated the use of avacopan in patients with GPA or MPA receiving standard therapy.New information has raised significant concerns regarding the integrity of the clinical data from the ADVOCATE trial. The concerns relate to how the data for the ADVOCATE trial was handled before TAVNEOS was authorized, creating uncertainty about the reliability of the efficacy evidence supporting the product’s benefit-risk profile.Due to the data integrity concerns, the ADVOCATE trial publication was retracted by the New England Journal of Medicine on June 29, 2026.Health Canada is currently reviewing this information and assessing its impact on the authorization of TAVNEOS in Canada. Information for consumersTAVNEOS is used to treat adults with conditions known as severe active anti-neutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis, which are rare autoimmune diseases that cause inflammation of blood vessels. They include granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA). TAVNEOS is used along with other medicines to treat these conditions.TAVNEOS was authorized in Canada after Health Canada reviewed the information available at the time, including the main clinical trial data used to support its use. Recently, new information has raised serious concerns about the reliability of that data, creating uncertainty about the evidence used to show how well TAVNEOS works. Health Canada is reviewing this information, together with the known risks of TAVNEOS, to determine whether its benefits continue to outweigh its risks.Patients should not stop taking TAVNEOS without first speaking to their healthcare professional. Patients currently taking TAVNEOS should contact their healthcare professional to discuss their treatment and whether another therapy may be appropriate. Information for healthcare professionalsPending the outcome of Health Canada’s review of these concerns, healthcare professionals are advised to:NOT initiate treatment with TAVNEOS in new patients.Contact and monitor patients currently receiving TAVNEOS and assess whether continued treatment remains appropriate. Action taken by Health CanadaHealth Canada is communicating this important safety information to healthcare professionals and Canadians via the Recalls and Safety Alerts Database on the Healthy Canadians Web Site. This communication will be further distributed through the MedEffect™ e-Notice email notification system. Report health or safety concernsManaging marketed health product-related side effects depends on healthcare professionals and consumers reporting them. Any case of serious or unexpected side effects in patients receiving TAVNEOS should be reported to Otsuka Canada Pharmaceutical Inc. or Health Canada.Otsuka Canada Pharmaceutical Inc. Address: 2250 Boul. Alfred Nobel, Suite 301 Saint-Laurent (Québec) H4S 2C9Telephone (Toll free): 1-877-341-9245 Fax: 1-844-268-9110Email: [email protected] or [email protected] To correct your mailing address or fax number, contact Otsuka Canada Pharmaceutical Inc.You can report any suspected adverse reactions associated with the use of health products to Health Canada by:Calling toll-free at 1-866-234-2345; orVisiting MedEffect Canada's Web page on Adverse Reaction Reporting for information on how to report online, by mail or by fax.For other health product inquiries related to this communication, contact Health Canada at:Pharmaceutical Drugs DirectorateE-mail: pharma_drug_enquiries-renseignements_medicaments_pharma@hc-sc.gc.ca Telephone: 613-957-0368Fax: 613-952-7756 Original signed by Achim ObergfellSenior Director, Medical Affairs, Cardiovascular & RenalVifor Fresenius Medical Care Renal Pharma
Gummy Gainz brand Protein Candy recalled due to improperly declared milk
The food recall warning issued on 2026-07-04 has been updated to include additional product information, marked by an asterisk (*). This additional information was identified during the Canadian Food Inspection Agency’s food safety investigation.The affected products are being recalled from the marketplace because they contain milk which is improperly declared on the label.
Rowenta Cordless Vacuum Cleaners recalled due to fire and burn hazards
The recalled lithium-ion battery in the vacuum cleaner can overheat and ignite, posing a risk of serious injury from fire and burn hazards.As of July 2, 2026, the company has received no reports of incidents or injuries in Canada.
Two lots of Omnitrope injectable human growth hormone recalled due to cracked cartridges
Sandoz Canada Inc. is recalling two lots of Omnitrope 5 mg/1.5 mL somatropin after receiving complaints of cracked and leaking glass cartridges. Cracked and leaking cartridges may lead to contamination and infection, and to lower doses than intended.Omnitrope is a prescription drug that contains somatropin, a human growth hormone that is administered by subcutaneous injection (under the skin). Omnitrope is used to treat both adults and children with growth hormone deficiency, and to treat children who have not reached or maintained normal growth by the age of two years, or who have Turner syndrome.Injecting contaminated Omnitrope subcutaneously may lead to local or systemic infection (i.e., near the injection site or throughout the body). Glass particles may cause local tissue irritation and may lead to local tissue infections or abscesses (pus-filled lumps). Lower doses of Omnitrope over a long period of time (weeks) may also reduce its effectiveness.Health Canada is monitoring the company's recall and investigation, including its implementation of corrective and preventive actions to prevent this issue from reoccurring, and will inform the public if new risks are identified.
The Butcher Barn brand meat products recalled due to undeclared mustard and soy
The affected products are being recalled from the marketplace because they contain mustard and soy which are not declared on the label.
Cuisinart Propel+ Four Burner 3-In-1 Gas Grills recalled due to a laceration hazard
The tempered glass window in the pizza oven can shatter during use, posing a risk of injury from laceration. As of June 25, 2026, the company has received 1 report of incident and no reports of injuries in Canada. In the United States, the company has received 37 reports of incidents and no reports of injuries.
ºM Warmer
A misplaced seal may cause leakage internally in the ºM Warmer device. This can lead to a shortcut of the electronics which may result in overheating. When the device and leaking fluids overheat, it has the potential for reaching temperatures that can cause burns (skin, nerve, Superficial Venous Thrombosis (SVT)) due to exposure to overheated device or fluid.
Insignia® Gas Ranges recalled due to fire hazard
The front mounted knobs on the recalled ranges can be activated by accidental contact by humans or pets, posing a fire hazard.As of June 17, 2026, the company has received no reports of incident or injury in Canada. In the United States, the company has received one report of knobs being activated by accidental contact and no reports of injuries.
Astral 150™
An internal electrical component (supercapacitor) may leak electrolyte over time. In rare cases, this may damage specific circuitry on the ventilator's Printed Circuit Board Assembly ("PCBA"), causing the ventilator to inadvertently enter a fail-safe state. In this state, the ventilator is no longer able to deliver therapy. Alternative means of ventilation must be provided.
Phantom® Hindfoot TTC/TC Ball Tipped Guide Rod
Zimmer Biomet Canada on behalf of Paragon 28, Inc. is conducting a lot-specific medical device recall removal of ball tipped guide rods used in the Phantom® Hindfoot TTC/TC Ball System. Two (2) complaints were received involving breaches in the sterile barrier of the pouch packaging. No clinical impact has been reported. The defectiveness was discovered on February 24, 2026. Issue was identified through the complaints handling process. Then the subsequent investigation followed that a recall would be required. On June 5, 2026 the manufacturer notified Zimmer Biomet Canada the need for a recall.
Chongqing Hot and Sour Sauce recalled due to undeclared peanut
The affected product is being recalled from the marketplace because it contains peanut which is not declared on the label.
Charcuterie Charlevoisienne and Joe Smoked Meat brand meat products recalled due to Listeria monocytogenes
The affected products are being recalled from the marketplace due to possible Listeria monocytogenes contamination.
Highgate Tender Meats Ltd. brand Honey garlic sausage recalled due to undeclared wheat
The affected product is being recalled from the marketplace because it contains wheat which is not declared on the label.
BD ChloraPrep™ Clear - 1mL Applicator: Product sterility
Product sterility could be compromised in affected lots.
Apo-Tiotropium Capsules; Out-of-specification (particle size)
The particle size did not meet the specifications in the affected lots.
Oribe Serene Scalp Densifying Shampoo; Presence of bacterial contamination
Affected lots may contain the presence of bacterial contamination (pluralibacter gergoviae).
Health Canada warns that BABESIDE Doll and Stroller Set previously available on Amazon.ca may pose a risk of choking
The eyes on the plush bear may detach and pose a choking hazard. The magnetic pacifier is a small part and may also pose a choking hazard.
Heavenly Spices brand Garlic Powder recalled due to Bacillus cereus
Heavenly Spices brand Garlic Powder recalled due to Bacillus cereus.
Presource ®Kits containing Teleflex Pilling® Wecksorb Neurosponge
Cardinal Health was recently informed of a medical device recall from Teleflex concerning the Pilling® Wecksorb Neurosponge referenced. The recall is being issued due to out-of-specification, or potential out-of-specification levels of endotoxin.
Leoni Plus
An electronic component may overheat internally.
Boon PIVOT Toddler Tower Kids Kitchen Step Stool recalled due to tip-over hazard
The stool may be unstable while in use, posing a tip-over hazard to users.As of July 9, 2026, the company has received no reports of incidents or injuries in Canada. In the United States, the company has received 11 reports involving the stools being unstable and no injuries have been reported.
Panasonic Flashxpress Toaster Oven recalled due to electric shock hazard
The power cord insulation may be insufficient due to a protective fiberglass sleeve not covering it adequately, which poses an electrical shock hazard to consumers.As of June 15, 2026, the company has received no reports of incident or injury in Canada. In the United States, the company has received 5 reports of circuit breaker tripping incidents involving the US model, but no incidents of shock or fire and no reports of injuries.
V-Loc™ 90 and 180 Suture Products
On 29-Jan-2026 during a quality inspection at a manufacturing site, a V-Loc 180 unit was found with a hole in the breather pouch on the Tyvek side. The breather pouch serves as the sterile barrier system for the suture. Investigation determined the briller plate on the sealing station may be causing the hole. No complaints have been identified for this issue, but lots within the issue bounding have been released to Distribution Centers (DCs) and sold to customers. These released lots may also contain units with holes in the Tyvek side of the breather pouch.
StrykeFlow PS and AHTO
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
SEMA 3
When an ECG is aquired with DEFIGARD Touch 7 or ARGUS PRO LifeCare 3 with the newest software, there might be a discrepancy between the aquiring device and SEMA. This results from inadequate processing by SEMA to an already filtered signal. SEMA should be updated to version 25.10.
Solar™ GI
Under extended clinical use conditions (e.g., long-duration studies), moisture generated within the pneumatic circuit may accumulate inside the system's internal tubing or at the hydrophobic filter (part of MPP T/PC tubing set) and pressure sensors. Accumulated moisture may affect airflow or pressure measurement performance if not properly removed. Water ingress in the air compressor can cause inaccurate pressure readings, resulting in excess fluid being administered to the patient than what is indicated by the system, which can lead to patient water intoxication. The issue is only related to Solar GI systems that have water perfusion capabilities.
Ola-Ola brand Authentic Pounded Yam (Iyan) IYANINSTANT recalled due to undeclared milk
The food recall warning issued on 2026-06-26 has been updated to include additional product information, marked by an asterisk (*). This additional information was identified during the Canadian Food Inspection Agency’s food safety investigation.The affected products are being recalled from the marketplace because they contain milk which is not declared on the label.
Various brands of meat products recalled due to Listeria monocytogenes
The affected products are being recalled from the marketplace due to possible Listeria monocytogenes contamination.
Mounit el Bait brand Tahina recalled due to undeclared peanut
The affected products are being recalled from the marketplace because they contain peanut which is not declared on the label.
Merge PACS
Merge PACS Dynamic Thumbnail Refresh feature may cause thumbnails from a previously opened patient study to display in the Thumbnail Bar of a different patient's study. As an immediate workaround, a configuration change disables automatic refresh of the Thumbnail Bar.
ER-Spec Single-Use Vaginal Speculum with LED Light Source
Units from specific lots of the ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small, may exhibit a plastic burr on the proximal plastic blade, near the integrated light source. The burr may introduce a potentially sharp plastic edge, in a contact region for both the patient and healthcare provider.
Atellica® CH Urine Albumin (UAlb)
Siemens Healthineers has confirmed, through the investigation of customer complaints, the potential for the following issues associated with processing Atellica CH Urine Albumin (UAlb) tests on Atellica CH and Atellica CI analyzers.• Falsely depressed Atellica CH Urea Nitrogen (UN_c) results• Falsely depressed Atellica CH Enzymatic Hemoglobin A1c (A1c_E) results• Increased rate of reaction cuvette QC failuresThese issues may impact quality control (QC), calibrators, and patient results for the UN_c and A1c_E assays across all sample types.
Goodfood brand meatball meals recalled due to undeclared egg and sesame
Goodfood brand meatball meals recalled due to undeclared egg and sesame.
Philips Achieva and Ingenia Systems
Philips has identified an issue where component failures in the gradient coil of the affected MR systems may act as a heat source with a potential to produce smoke and/or fire. If a component failure occurs, the user may observe the following: repeated scan abort error messages due to gradient amplifier fault detection unusual noise from the system in the examination or technical room burning smell smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or death. This issue could also lead to property damage. The scope includes MR systems with gradient coil types WA15, WA30S, WB30S, and AG30S. Recall start date: July 7, 2025
Michley brand Children’s Pajamas recalled due to flammability hazard
The Michley-branded children’s pajamas violate the flammability requirements for children’s sleepwear, posing a risk of burn injuries to children.Loose-fitting children’s sleepwear can contact ignition sources such as stove elements, candles, and matches more readily than tight-fitting sleepwear, and once ignited will burn rapidly, potentially resulting in severe burns to large areas of the child’s body.For information on what makes safe sleepwear, visit the Healthy Canadians Children’s sleepwear safety page.As of July 16, 2026, the company has received no reports of incident or injuries in Canada.
RAINS Stainless Steel Tumbler recalled due to burn hazard
The plastic lid may detach unexpectedly and release hot liquid from the flask, posing a burn hazard.As of July 15, 2026, the company has received no reports of incident or injury in Canada.
10392804 Canada Inc. d.b.a Sweet Vengeance recalls certain edible cannabis products due to undeclared milk and hazelnut, and labelling issues
The affected chocolate products are being recalled because they contain milk and hazelnut which are not declared on the label. If you are allergic or sensitive to milk and hazelnut, consumption of the affected recalled products may cause a serious or life-threatening reaction.The labels for the affected products have incorrect cannabinoid values. The labels of chocolate products show that the THC is higher than the actual value. The label of cannabis product THC: CBD 1:25 Micro-dosed Vegan Chili Crisp shows that the THC is lower than the actual value. Without knowing the accurate THC level in the product, it could be difficult to make informed decisions regarding your cannabis use. This may lead to over-intoxication and temporary adverse health consequences associated with THC overdose, which could include:confusiondisorganized thinkingphysical and mental impairmentanxietyfear or panicdecreased blood pressureelevated heart rate
M & B SALT REMOVER recalled due to risk of potential rupture hazard
The pressurized container may experience mechanical failure (rupture) due to internal corrosion of the can. As of July 14, 2026, the company has received 3 reports of incidents and no reports of injury in Canada.
Shades and Alternating Blinds with a chain and cord-shield from Prime Custom Blinds recalled due to strangulation hazard
Health Canada has determined that the recalled blinds do not meet the Corded Window Coverings Regulations and pose a strangulation hazard. Young children may pull looped cords around their neck, or become entangled in the cords, causing a strangulation hazard and even death. Health Canada recommends cordless window coverings. For more information on the hazard, see Window Covering Safety page. As of July 14, 2026, the company has received no reports of incident or injury in Canada.
DCA Vantage® HbA1c (DX Claim)
Siemens Healthineers has confirmed through customer complaint investigation and internal testing that delamination of the buffer pull-tab may occur in a small subset of cartridges. Delamination occurs when bonded material layers within the pull-tab separate, preventing full release of the buffer solution into the reaction chamber and reducing the reagent volume available for analysis.When delamination occurs, it may result in falsely low (negatively biased) HbA1c results or instrument-generated error codes that prevent completion of the test. The issue observed in approximately 0.07-0.5% of cartridges in these lots. The majority of the cartridges in these lots continue to perform as intended.
HeartSine® Samaritan® PAD SAM 350P/SAM 360P/SAM 500P
Stryker has identified a limited number of HeartSine samaritan PAD devices that were distributed without the required maintenance supplement. This supplement contains periodic maintenance instructions implemented as an additional risk-control measure. While most devices contain the maintenance supplement, this voluntary correction is being initiated to ensure all end users have access to supplemental maintenance information. This issue was identified through a customer complaint.
Westside Sauce brand Peanut Thai recalled due to spoilage
Westside Sauce brand Peanut Thai recalled due to spoilage.
Izem Energy brand “Boisson énergisante gazeuse” recalled due to labelling issues
Izem Energy brand “Boisson énergisante gazeuse” recalled due to labelling issues.
Briine brand Pacific Tide Sparkling Spring Water recalled due to bulging cans
Briine brand Pacific Tide Sparkling Spring Water recalled due to bulging cans.
OverStitch™ Suture Cinch and Suture Cinch–Long
Boston Scientific is initiating removal of specific lots of OverStitch™ Suture Cinch and Suture Cinch-Long (collectively "Suture Cinch"). these devices are accessories used with the OverStitch™ Endoscopic Suturing System, OverStitch™ NXT Endoscopic Suturing System, and the X-Tack™ Endoscopic HeliX Tacking System to secure and cut the proximal end of a suture through the working channel of a gastroscope or colonoscope.During device activation, the Suture Cinch may fail to deploy the cinch implant and/or fail to cut the suture as intended. The issue cannot be detected through pre-use inspection but becomes apparent once the user attempts to deploy the device during the procedure.
HeartSine® Samaritan® PAD SAM 350P/SAM 360P/SAM 500P - Membrane Tail
Stryker has recently identified an issue with the membrane tail, an internal component, which could cause an intermittent fault. This failure could occur at any point when the device is holding a charge in preparation to deliver therapy, while delivering a shock, or after shock delivery. The device becomes inoperable after the failure occurs.
Izem Energy brand energy drinks recalled due to labelling issues
Izem Energy brand energy drinks recalled due to labelling issues.
Cadbury brand Dairy Milk Oreo Candy (bar) recalled due to undeclared pistachio
The affected products are being recalled from the marketplace because they may contain pistachio which is not declared on the label.
Fromagerie P. Jacquin & Fils brand Valençay AOP "fromage de chèvre au lait cru" recalled due to generic E. coli
Fromagerie P. Jacquin & Fils brand Valençay AOP "fromage de chèvre au lait cru" recalled due to generic E. coli.
Sphere-9™ Catheter
There have been forty-six (46) reported incident reports (none of which were from Canada) where patients with a Biotronik ICD experienced induced ventricular arrhythmia (VT and/or VF) following RF ablation of cardiac tissue using the Affera Sphere-9 catheter.Sphere-9 presents a higher current flow to the ICD or CRT-D which interacts with a safety feature built into Biotronik ICDs and CRT-Ds. The higher currents of the Sphere-9 catheter during RF application proceed to an unfavorable modulation of the coupled currents (approx. 40Hz frequency) that may be conducted via the implanted leads, and result in possible VT or VF induction.
Spacelabs Healthcare Xhibit® Central Station
Spacelabs Healthcare has concluded that the use of the previously distributed splitter (part number 010-1975-00) can have an adverse effect on product performance, specifically around audible and visible alarms. Splitters may fail to perform as intended and result in degraded or complete loss of alarm audio and video. Additionally, customer's own use of unqualified splitters may pose the same risks.
Harmonic Arts Holy Basil Tincture; Out of Specification (total aerobic microbial count)
The total aerobic microbial count is out of specification in the affected lot.
Rexall and Pro-Line chemical products recalled due to lack of child-resistant packaging
The recalled products do not meet the child-resistant packaging requirements of the Consumer Chemicals and Containers Regulations, 2001 under the Canada Consumer Product Safety Act. The lack of child-resistant packaging could result in unintended exposure to the products and lead to serious illness or injury. As of March 30, 2026, the company has received no reports of incidents or injuries in Canada.
Our Finest brand Shrimp Ring with Mild Cocktail Sauce recalled due to 3-amino-2-oxazolidinone
Our Finest brand Shrimp Ring with Mild Cocktail Sauce recalled due to 3-amino-2-oxazolidinone.
Divya brand Cumin Powder recalled due to presence of sand
Divya brand Cumin Powder recalled due to presence of sand.
Azurion Systems
Philips has identified two software-related issues affecting Azurion R2.x.10, R3.0, R3.1 and R4.0 systems that may result in delay of therapy, procedural complications and/or inappropriate treatment.Issue 1: Image quality degradationIssue 2: Loss of geometry movements - Applicable to systems with an AD7X table only
BenQ GV31 Portable Projector recalled due to burn and fire hazard
The portable projector may overheat, posing a risk of burn and fire hazards. As of June 23rd, 2026, the company has received no reports of incidents or injuries in Canada and one report of an overheating incident in the United States.
Pharmasave Regular Strength Dairy Digestive Supplement Lactase Enzyme: Affected lot is labelled with the incorrect Natural Product Number (NPN) on the carton.
Affected lot is labelled with the incorrect Natural Product Number (NPN) found on the carton. The correct NPN can be found on the bottle.
Femyso: Affected lot may contain two green Mifepristone cartons or two pink Misoprostol cartons instead of one of each.
Affected lot may contain two green Mifepristone cartons or two pink Misoprostol cartons instead of one of each.
Health Canada warns that TQELFSS Crystal Clear Epoxy Resin Kits previously available on Amazon.ca may pose a risk of serious illness or injury due to improper labelling.
Health Canada has determined that the TQELFSS Crystal Clear Epoxy Resin Kits do not meet the labelling requirements of the Consumer Chemicals and Containers Regulations, 2001 under the Canada Consumer Product Safety Act. The lack of appropriate labelling information could result in unintentional exposure to the products and lead to serious illness or injury.
Hershey's brand Kisses - Creamy Milk Chocolate recalled due to undeclared almond
The affected products are being recalled from the marketplace because they may contain almonds which are not declared on the label.
Coaticook brand White Cheddar cheeses recalled due to Listeria monocytogenes
The affected products are being recalled from the marketplace due to possible Listeria monocytogenes contamination.
Highline brand Organic Mini Bella Mushrooms Sliced recalled due to Listeria monocytogenes
The affected product is being recalled from the marketplace due to possible Listeria monocytogenes contamination.
Ultra Big Blue Automatic Toilet Bowl Cleaner recalled due to improper labelling and lack of child-resistant packaging
The recalled product does not meet the labelling and child-resistant packaging requirements of the Consumer Chemicals and Containers Regulations, 2001 under the Canada Consumer Product Safety Act.The lack of appropriate labelling information and child-resistant packaging could result in unintentional exposure to the products and lead to serious illness or injury including death.As of July 28, 2026, the company has received no reports of incident or injury in Canada.
Needle Kit For Powered Driver
Some lots were manufactured with out-of- tolerance dimensions, and as a result some users have reported difficulty removing the obturator (stylet) following placement of the BD Intraosseous Vascular Access System Needle Sets. Based on complaint reports, bench testing completed by BD and clinical observations, this may occur when pulling back on the drill during the insertion or when failing to pull straight back with the powered driver or incorrectly rotating or trying to unscrew the obturator. These actions allow the rotation and locking of the obturator-needle hub interface for specific lots of the product with out-of-tolerance dimensions.
Flow brand Organic Flavoured Mineral Spring Water - Peach + Blueberry recalled due to mould
Flow brand Organic Flavoured Mineral Spring Water - Peach + Blueberry recalled due to mould.
RELLET Hyaluronic Acid Deep Hydrating Spray recalled due to missing mandatory hazard labelling
The recalled products do not have mandatory hazard labelling as required by the Cosmetic Regulations under the Food and Drugs Act. Improper labelling could result in misuse of the product and lead to serious injury.As of July 31, 2026, the company has received no reports of incidents or injuries in Canada.
Kehar brand Californian Pistachio Kernel recalled due to Salmonella
The affected products are being recalled from the marketplace due to possible Salmonella contamination.
Compliments brand Smashed 100% Chicken Burgers recalled due to undeclared egg
Compliments brand Smashed 100% Chicken Burgers recalled due to undeclared egg.
Louisville and Featherlite brand Attic Stairways recalled due to injury hazard
The 1/4-inch chrome-colored bolts used in the spreader assembly on Louisville and Featherlite attic stairways manufactured on or before June 22, 2026, may not meet Louisville Ladder Corp.'s design specifications, posing a potential injury hazard.As of July 24, 2026, the company has received 1 report of an incident and no reports of injuries in Canada. In the United States, the company has received 11 reports of incidents and 1 report of an injury.
DR Power PRO MAX30 30” Deck Wide Cut Walk-Behind Power Lawn Mowers recalled due to laceration hazard
The blades of the lawn mower can operate without the blade control system engaged or continue to operate even after the release of the control, posing a serious laceration hazard. As of July 28, 2026, the company has received no reports of incident or injury in Canada. In the United States, the company has received 19 reports of incidents and no reports of injuries.
CCM Hybrid Visor and Replacement Visor accessory recalled due to impact hazard
CCM has determined that these products do not fully align with the company's current manufacturing quality standards. CCM has therefore decided to initiate a voluntary product recall for these products.The polycarbonate portion of the hybrid visor may in some cases develop micro-fissures around the screw holes that connect the polycarbonate portion to the cage portion, which could potentially lead to cracking if it were subject to a powerful impact, such as a puck travelling at high velocity.As of July 17, 2026, the company has received no reports of incident or injury in Canada.
One lot of New Roots Herbal Probiotic Intensity recalled due to incorrect “No Dairy” claim
New Roots Herbal Inc. is recalling one lot of Probiotic Intensity because the outer box of the 30-count bottles incorrectly states that the product contains no dairy. The product contains bovine colostrum, which is a dairy ingredient. Bovine colostrum may pose serious health risks to people with a severe dairy allergy.Although the labelling issue affects only the 30-count bottles, the company is recalling the entire lot, which also includes 60-count bottles. The recalled lot was distributed starting in October 2025.People with allergies to dairy (e.g., milk) can experience a range of mild to severe symptoms when exposed to even small amounts of milk proteins. These symptoms may include raised and itchy bumps on the skin, upset stomach, and breathing difficulties that can be life threatening.Probiotic Intensity is intended for adults and children aged six years and older to support intestinal and gastrointestinal health and immunity.Health Canada is monitoring the company's recall and investigation, including its implementation of corrective actions to prevent this issue from reoccurring, and will inform the public if new risks are identified.
HEALON EndoCoat PRO
Johnson & Johnson Surgical Vision, Inc. is issuing a voluntary recall notice for HEALON EndoCoat™ PRO to inform customers of reports involving difficulty with insertion of the ultra-thin 25g orange cannula. This notice is intended to communicate the potential risks associated with cannula insertion and provide additional clarification regarding insertion technique to support the safe and effective use of the product. This recall does not require removal or return of the product from the market. When used in accordance with the instructions provided in this notice, the product may continue to be used as intended.
Beckman Coulter AU Immunochemistry System - AU480 Analyzer
Beckman Coulter has determined that a software defect in AU480 chemistry analyzers using Microsoft® SQL server 2022 express may cause a DB connection error that renders alarmDB unreadable and prevents instrument startup. The issue is associated with transaction log auto-growth, and may cause delays in reporting patient test results to physicians.
TEVA-ECTOSONE 0.1% Cream; Affected lot may be missing lot number and expiry date
Affected lot may be missing the lot number and expiry date on the label.
Momchipz brand Veggie Chips (Broccoli Florets & Cauliflower) recalled due to undeclared gluten
The affected product is being recalled from the marketplace because it contains gluten which is not declared on the label.
Bravo - Capsule Delivery System
Medtronic has identified an increase in complaints involving the Bravo CF capsule delivery device where the capsule fails to attach to the esophagus or detach from the delivery device. Medtronic's preliminary root cause investigation has identified a potential condition impacting the component that controls the deployment of the capsule which can then be exacerbated by a failure to keep the delivery device straight as instructed in the user guide, as a potential cause. Risks associated with this issue include patient aspiration/inhalation, perforation of esophagus, obstruction of the airway, hemorrhage/blood loss/bleeding, laceration of the esophagus, a delay in diagnosis, and foreign bodies remaining in the patient.Lots with an expiration date of December 10, 2027, or later are not in scope of this recall and do not need to be returned.
PC Organics brand and Frankie's Organic brand Plant-based cheddar corn puffs and crunchies recalled due to undeclared milk
The affected products are being recalled from the marketplace because they contain milk which is not declared on the label.
Corded zebra window covering / zebra blind recalled due to strangulation hazard and choking hazards
Health Canada has determined that the recalled window covering do not meet the Corded Window Coverings Regulations and pose a strangulation hazard and a choking hazard. Young children may pull looped cords around their neck, or become entangled in the cords, causing a strangulation hazard and even death. The window covering could potentially release small parts that present a choking hazard to young children.Health Canada recommends cordless window coverings. For more information on the hazard, see Window Covering Safety page.As of July 31, 2026, the company has received no reports of incident or injury in Canada.
Omni-Tract Surgical Retractor System
Integra Lifesciences is issuing a correction to the Integra® Omni-Tract® Surgical Retractor System - existing Instructions For Use (IFU) related to prevacuum sterilization dry time requirements, to ensure the Omni-Tract® devices and components are properly dried during sterilization to qualify current ISO standards. The current Omni-Tract® Surgical Retractor System IFU states a dry time of 30 minutes. The validated drying times utilizing standard pre-vacuum temperature and time standards were significantly longer and needed to be extended to 90 minutes, 110 minutes, or 120 minutes depending on the sterilization cycle exposure time used.Update: Integra LifeSciences is issuing this additional updated correction to the Integra® Omni-Tract® Surgical Retractor System - Instructions for Use (IFU) adding prevacuum sterilization parameters when using a rigid container. Previously, in our June 2026 communication, Integra LifeSciences provided drying times solely for polypropylene wrapped sterilization trays informing you of three (3) the dry times (90 minutes, 110 minutes, or 120 minutes) depending on the sterilization cycle exposure time. This updated notification contains additional sterilization testing validated using a rigid container with the updated prevacuum sterilization cycle parameters.
Alfa brand croissant products recalled due to mould
Alfa brand croissant products recalled due to mould.
Portable Clip-On Rechargeable Mini Fan recalled due to fire hazard
The recalled fan has a battery compartment that is not sealed or labelled with clear polarity markings which could lead the consumer to insert a battery in reverse polarity, posing a potential fire hazard.As of July 26, 2026, the company has received 1 report of an incident and no reports of injury in Canada.
Portrait Core Services Cssxb
GE HealthCare has become aware that during a service event to update Portrait Core Services software at a facility, patients who are monitored on Portrait Mobile devices can be discharged from the Portrait monitoring system.
Certain Whole Foods Market brand guacamoles, pico de gallos, salsas, and prepared foods recalled due to Salmonella
The affected products are being recalled from the marketplace due to possible Salmonella contamination.This recall is associated with an Outbreak Investigation of Salmonella: Jalapeño (August 2026) | FDA
Aqua Gems brand Tempura Shrimp recalled due to undeclared egg
Aqua Gems brand Tempura Shrimp recalled due to undeclared egg.
Zhou Hei Ya brand Wide Vermicelli with Sesame Sauce recalled due to undeclared shrimp
The affected product is being recalled from the marketplace because it contains shrimp which is not declared on the label.
Taleco Gear 2-in-1 Jumper & Swing-A recalled due to fall and strangulation hazards
The products may become unstable, posing fall and impact hazards. Hanging straps and seat openings may pose strangulation risk.As of July 28, 2026, the company has received no reports of incident or injury in Canada. In the United States, the company has received 52 reports of incidents including 32 reports of injuries.
Baby walkers sold at ToyTexx (Richmond Hill location) recalled due to physical hazard
Baby walkers have been banned in Canada since 2004.Children in baby walkers are exposed to hazards that would not normally be accessible if the child were not supported by the walker, posing a variety of risks of injury to the child. Children in baby walkers can also fall down the stairs, which could result in injury or death.As of August 5, 2026, the company has received no reports of incident or injury in Canada.
Roller Blinds in a Cassette by Omni Blinds recalled due to strangulation hazard
Health Canada has determined that the recalled blinds do not meet the Corded Window Coverings Regulations and pose a strangulation hazard. Young children may pull looped cords around their neck, or become entangled in the cords, causing a strangulation hazard and even death. Health Canada recommends cordless window coverings. For more information on the hazard, see Window Covering Safety page. As of August 4, 2026, the company has received no reports of incident or injury in Canada.
Various Salem Foods brand jarred products recalled due to undeclared wheat, mustard and sesame
Various Salem Foods brand jarred products recalled due to undeclared wheat, mustard and sesame.
Coaticook brand Mild Cheddar Curds - White, Frozen recalled due to Listeria monocytogenes
Coaticook brand Mild Cheddar Curds - White, Frozen recalled due to Listeria monocytogenes.
Clément le Gourmand brand meat products recalled due to Listeria monocytogenes
The affected products are being recalled from the marketplace due to possible Listeria monocytogenes contamination.
Warn® wireless remote kit for truck and utility winches recalled due to failure to operate
The wireless receiver modules may be incompatible with certain legacy winches equipped with individual solenoid-type control packs, posing risk of damage to the wireless receiver and failure of the winch to stop when commanded. As of July 17, 2026, the company has received no reports of incident or injury in Canada.
Madewell Double V-Neck Pullover and V-Neck Cardigan Sweaters recalled due to flammability hazard
The recalled V-Neck Pullover and Cardigan Sweaters do not comply with flammability requirements of the Textile Flammability Regulations, posing a burn hazard to consumers. As of July 30, 2026, the company has received no reports of incident or injury in Canada.
Orthopaedic Implant Components
Stryker has become aware that the devices listed in the Customer Letter were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five (5) years. Industry guidance for storage duration of UHMWPE raw material used in the manufacture of implant bearing/articulating material of prosthetic joints is less than five (5) years. Product manufactured using UHMWPE raw material beyond the recommended storage duration has the potential for elevated levels of oxidation. Oxidation of UHMWPE material can impact material properties, potentially resulting in increased wear.
Endotracheal Tube, Cuffed
The 6FR suction catheter could not pass smoothly through the 2.5mm sizes of cuffed tracheal tube. This may lead to reintubations if the airway is unable to be suctioned.To date, there have been two complaints reported from united states customers where one required reintubation. No serious patient harm has occurred.
Two lots of Teva-Pregabalin 150 mg capsules recalled due to cross-contamination with the drug sertraline
Teva Canada Ltd. is recalling two lots of Teva-Pregabalin 150 mg capsules after routine testing identified that some capsules may be contaminated with the drug sertraline. Patients with a hypersensitivity or allergy to sertraline could experience side effects or have a serious allergic reaction, including an anaphylactic reaction, even at a low exposure. Anaphylactic reaction symptoms can be fatal and may include: Shortness of breath, wheezing, or difficulty breathing Swelling of the eyelids, face, lips, mouth, tongue, or throat Uncontrolled shaking Fainting or dizziness Trouble swallowing or speaking Widespread rash, hives Products from the recalled lots were first sold in Canada in September 2025 and expire July 31, 2027. Pregabalin is a prescription drug used in adults to treat pain caused by nerve damage due to diabetes, shingles or spinal cord injury. It is also used to treat pain associated with fibromyalgia. Sertraline is a prescription drug used in adults to relieve symptoms of depression, obsessive-compulsive disorder, and panic disorder. Side effects may include nausea, diarrhea, dry mouth, sleep changes, dizziness, tremors or increased sweating. Health Canada is monitoring the company's recall and implementation of corrective and preventive actions.
Various brands of cheese products recalled due to generic E. coli
Various brands of cheese products recalled due to generic E. coli.
Olymel brand Cooked Turkey Breast Roast Honey & Dijon recalled due to incorrect labelling and undeclared mustard
Olymel brand Cooked Turkey Breast Roast Honey & Dijon recalled due to incorrect labelling and undeclared mustard.
Lactated Ringer's Injection USP: Presence of Particulate Matter
Presence of particulate matter in affected lot
Cook Medical Hemospray Kit
A communication is being issued to customers to provide information to be included in an upcoming change to the Instructions for Use. The additional information provides added details intended to reduce the risk of potential endoscope adherence and inability to spray powder.
Unauthorized drugs seized from Rabais 4Saisons Inc. in Montreal, QC, may pose serious health risks
Health Canada has seized several unauthorized drugs (including an oral emergency contraceptive drug, erectile dysfunction drugs, and antibiotic and antiparasitic drugs) from Rabais 4Saisons Inc. (5321 rue de Charleroi), in Montreal, Quebec, because they may pose serious health risks. Selling unauthorized health products in Canada is illegal. Unauthorized health products have not been approved by Health Canada, which means they have not been assessed for safety, effectiveness and quality and may pose serious health risks. For example, they may lack active ingredients, vary in their concentration or contain ingredients, additives or contaminated ingredients not listed on the label that could interact with other medications and foods. Many of the seized products are unauthorized versions of prescription drugs available in Canada. Prescription drugs should be used only under the supervision of a health care professional because they are used to treat specific conditions and may cause serious side effects. Several of the products are not labelled in English and French as required in Canada. As a result, information about ingredients, usage, dosage and side effects may not be available to or understood by consumers. Health Canada acts to protect public health and safety when companies are found to be selling unauthorized health products in Canada, including warning consumers when warranted. The Department also works with the Canada Border Services Agency to help prevent the import of any unauthorized health products.
Wu Xian Zhai brand Vegetarian beef and Preserved beancurd recalled due to undeclared wheat
The affected products are being recalled from the marketplace because they contain wheat which is not declared on the label.
Custom made 3-inch black fascia manual roller shade manufactured by Greystone Blinds recalled due to strangulation and choking hazards
Health Canada has determined that the recalled manual roller shades do not meet the Corded Window Coverings Regulations and pose a strangulation hazard. Young children may pull looped cords around their neck, or become entangled in the cords, causing a strangulation hazard and even death. In addition, the products can also release small parts that present a choking hazard to young children. Health Canada recommends cordless window coverings. For more information on the hazard, see Window Covering Safety. As of August 10, 2026, the company has received no reports of incidents or injuries in Canada.
Embosphere® Microspheres-Syringe
Merit Medical Systems, Inc., on behalf of its subsidiary, Biosphere Medical, is voluntarily recalling specific lots of the Merit Embosphere® Microspheres due to a supplier-related defect that may affect the device packaging sterile barrier. Specifically, certain lots provided to Merit may contain a hole in the blister packaging. Merit has chosen to remove the units from the market and request that customers immediately stop using or distributing the affected lots and return the affected product to Merit. According to Merit's evaluation of health hazard(s), use of the affected product may result in exposure to pathogens/pyrogens, which could lead to infection. To date, Merit has not received any complaints or reports of patient harm or injury associated with this issue.
SPECTRALIS® with Flex Module
There is a possibility that the castor wheels of the Flex stand are not properly attached. The wheels may come loose. As a result, the Flex stand may tip over. Users shall schedule a service appointment as soon as possible so that the castor fastenings can be inspected and corrected.
StatStrip® Glucose And Beta-Ketone Hospital Meter
A software issue in StatStrip (Gen 2) Glucose and Beta-Ketone Hospital Meters may retain previous patient information during barcode scanning, potentially assigning results to the wrong patient. Users should verify patient identification before accepting scanned data and follow the correction instructions provided by Nova Biomedical.
Workbless Electric Pressure Washers recalled due to electric shock hazard
The recalled electric pressure washers lack a ground fault circuit interrupter (GFCI) and the power cord is too short which may encourage the use of an extension cord, posing a risk of an electric shock hazard. As of August 14, 2026, the company has received no reports of incident or injury in Canada or in the United States.
MEC Shuttlecraft Kid Carrier recalled due to potential fall hazard
The black plastic component at the adult shoulder strap attachment point of the frame can fracture, which may cause the adult shoulder strap to slip off, posing a potential fall hazard to the child. As of August 11, 2026, the company has received no reports of incident or injury in Canada.
Centricity™ Enterprise Archive and PACS Workstation
GE Healthcare has become aware that, under certain conditions, historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the wrong patient record, which could lead to misdiagnosis or a delay in patient care.
Patient Information Centre iX
Philips received reports that some PIC iX systems were frozen and could not be used. It was determined that failure of the watchdog may cause the system to be in an unknown state and therefore potentially prevent alarms from being generated or logged. Following the initial system error which triggers the watchdog, staff may observe unexpected system behavior while the watchdog attempts recovery. The observed behavior depends on the underlying software issue and may include:-Inability to interact with the PIC iX user interface. If real-time waveforms, numeric data,and alarms remain operational, there is no impact to bedside or central monitoring and alarming.-The user will not recognize the device issue before the hazardous situation occurs if theobserved behavior is: Loss of central alarming, Loss of, or frozen, waveforms/data display-Bedside monitors and telemetry devices could generate a "No Central Mon" INOP
Theragun PRO
The charger of the Theragun G4PRO massage device can overheat while charging the device's removable battery pack, presenting the risk of a potential thermal event. Consumers should stop using the charger immediately and contact Therabody, Inc. to receive a replacement charger or credit code. The Theragun G4PRO itself is not affected by the recall but it cannot be used with other chargers.
OneTang brand Walnut Soft Candy with Black Sesame recalled due to presence of stones
OneTang brand Walnut Soft Candy with Black Sesame recalled due to presence of stones.
Compliments brand and Selection brand Corn Dogs recalled due to Listeria monocytogenes
Compliments brand and Selection brand Corn Dogs recalled due to Listeria monocytogenes.
Kim Phat brand Seafood Medley recalled due to undeclared egg, fish, soy, and wheat
The affected product is being recalled from the marketplace because it contains egg, fish, soy, and wheat which are not declared on the label.
Health Canada warns that Baby Activity Walker previously available on Fruugo.ca may pose a risk of injury
Baby walkers are banned in Canada. Children in baby walkers are exposed to hazards that would not normally be accessible if the child were not supported by the walker, posing a variety of risks of injury to the child. Children in baby walkers can also fall down the stairs, which could result in injury or death.
Health Canada warns that Oversized Heightened Kids Walking Rehabilitation Walker previously available on AliExpress may pose a risk of injury
Baby walkers are banned in Canada. Children in baby walkers are exposed to hazards that would not normally be accessible if the child were not supported by the walker, posing a variety of risks of injury to the child. Children in baby walkers can also fall down the stairs, which could result in injury or death.
Health Canada warns that MUELODSIC - Multifunctional Walker previously available on Amazon.ca may pose a risk of injury
Baby walkers are banned in Canada. Children in baby walkers are exposed to hazards that would not normally be accessible if the child were not supported by the walker, posing a variety of risks of injury to the child. Children in baby walkers can also fall down the stairs, which could result in injury or death.
ForeSight™ Oximeter Cable
This recall is regarding inaccurate StO2 readings from the HEMFSM10 ForeSight™ Oximeter Cable due to mispositioning of the sensor cables. Edwards has identified that during manufacturing, the laterality identification labels may be missing or inaccurately placed on the device. There is potential that the labels on the green cables may have been switched, with the channel 1 cable labeled as channel 2, and the channel 2 cable labeled as channel 1. This will lead to a mismatch as to the left and right values displayed on the monitor and what the labels indicate on the cables. Should this potential issue occur during use, the values displayed on the monitor will be switched and will represent the opposite region being monitored. Therefore, there is a potential for incorrect diagnosis, leading to potential delay of appropriate treatment. If either of the labels are missing, or the flag label and/or the sensor label do not match the channel label on the housing, contact the Technical Support. If the flag and sensor labels correctly correspond to the channel labels, there is no further action required.
Aisys™ CS² and Carestation™
The Aisys™ Carestation™ Anesthesia System, Aisys™ CS² and Aisys™ CS² with Et Control, containing certain electronic gas mixer assemblies, can automatically transition to Alternate O2 Control.
iQ200 Series Analyzers and DxU 840m/850m Iris Analyzers
Beckman Coulter received customer complaints of lamina fluid leaks in iQ200 Series and DxU 840m/850m Analyzers. The investigation found that a structurally compromised rinse-line check valve may allow fluid to migrate internally and leak onto the table or floor, potentially resulting into exposure to physical or mechanical or chemical hazards.
SANA brand manually controlled solar shades recalled due to strangulation hazard
Health Canada has determined that the recalled blinds do not meet the Corded Window Coverings Regulations due to non-compliance of the tension device supplied with the product and pose a strangulation hazard. Young children may pull looped cords around their neck, or become entangled in the cords, causing a strangulation hazard and even death. Health Canada recommends cordless window coverings. For more information on the hazard, see Window Covering Safety. As of August 7, 2026, the company has received no reports of incident or injury in Canada.
Importation of South Korean-Authorized BONKY Injection, 1 mcg/mL Calcitriol, due to the Current Shortage of Canadian-Authorized Calcitriol Injection USP, 1 mcg/mL
There is a shortage of Calcitriol Injection USP in Canada. Given the medical necessity of Calcitriol Injection USP, 1 mcg/mL and the need to maintain continuity of supply in Canada, Health Canada has authorized the exceptional, temporary importation and sale of South Korean-authorized BONKY Injection, 1 mcg/mL Calcitriol, with Korean-only labels to mitigate the shortage. Healthcare professionals should be aware that there are differences between the South Korean-authorized and Canadian-authorized products (see Information for healthcare professionals section). Audience Healthcare professionals at hospitals and units such as dialysis clinics and renal units. Key messages Due to a shortage of Calcitriol Injection USP, 1 mcg/mL in Canada, and given the medical necessity of this drug, Health Canada has permitted the exceptional, temporary importation and sale of South Korean-authorized BONKY Injection, 1 mcg/mL Calcitriol with Korean-only labels. This South Korean-authorized product has the same active ingredient (calcitriol), strength (1 mcg / mL), dosage form (injection), and route of administration (intravenous) as the Canadian-authorized product. However, there are differences between these products. Healthcare professionals are advised that: The South Korean-authorized product has a different brand name, carton and ampoule label, and pack size (10 x 1 mL ampoules instead of 25 x 1 mL ampoules) than the Canadian-authorized product (see Appendix 1). The expression of strength displayed on the South Korean-authorized product carton appears as “1 µg”, whereas the South Korean-authorized ampoule displays the strength as “1 mcg/mL”. Please note that “µg” denotes microgram (mcg). Refer to the expression of strength displayed on the ampoule label when verifying the product strength. The Canadian-authorized product displays the strength as “1 mcg/mL” on both the carton and ampoule. Although the South Korean-authorized product has differences in carton and ampoule labelling, healthcare professionals should continue to consult the Indications, Contraindications, Warnings and Precautions, Adverse Reactions, Dosage and Administration, and Storage Conditions sections of the Canadian Product Monograph for Calcitriol Injection USP, 1 mcg/mL by SteriMax Inc. (DIN 02399334), available in English and French on Health Canada’s Drug Product Database. Pharmacies/hospitals are advised to generate a sticker or auxiliary label for the outer carton label (and ampoules, if feasible) to ensure proper identification of the product and access to safe use information (including the active ingredient and strength using mcg/mL). Background Information In Canada, Calcitriol Injection USP is indicated for the management of hypocalcemia in patients undergoing chronic renal dialysis. It has also been shown to help with the improvement of renal osteodystrophy by reducing elevated parathyroid hormone levels. Calcitriol Injection USP is NOT recommended for use in pediatric patients. Currently, there is a critical shortage of Canadian-authorized Calcitriol Injection USP, 1 mcg/mL in Canada. To help mitigate the shortage, Health Canada has permitted the exceptional, temporary importation and sale of South Korean-authorized BONKY Injection, 1 mcg/mL Calcitriol, with Korean-only labels. Information for healthcare professionals The South Korean-authorized product has the same active ingredient (calcitriol), strength (1 mcg/mL), dosage form (injection), and route of administration (intravenous) as the Canadian-authorized product. However, there are differences between these products. Healthcare professionals are advised that: The South Korean-authorized product has a different brand name, carton and ampoule label, and pack size (10 x 1 mL ampoules instead of 25 x 1 mL ampoules) than the Canadian-authorized product (see Appendix 1). Proper selection of the intended product must be verified to avoid confusion with other products and to prevent medication errors. The expression of strength displayed on the South Korean-authorized product carton appears as “1 µg”, whereas the South Korean-authorized ampoule displays strength as “1 mcg/mL”. Please note that “µg” denotes microgram (mcg). Refer to the expression of strength displayed on the ampoule label when verifying the product strength. The Canadian-authorized product displays the strength as “1 mcg/mL” on both the carton and ampoule. The labelling of the Canadian-authorized product includes the statement “NOT recommended for use in children”. While this information is not stated on the labels or in the translated prescribing information, the same applies to the South Korean-authorized product. The South Korean-authorized product label includes a serious warning that when opening an ampoule, glass fragments may enter the solution and cause adverse effects. The ampoule should be opened carefully to minimize contamination by glass fragments. The Canadian Product Monograph for Calcitriol Injection USP, 1 mcg/mL from SteriMax Inc. (DIN 02399334), available in English and French on Health Canada’s Drug Product Database, should be consulted for information on the appropriate use of the product, including the Indications, Contraindications, Warnings and Precautions, Adverse Reactions, Dosage and Administration, and Storage Conditions. The product labels of the Canadian-authorized Calcitriol Injection USP identify that the product is preservative free, sterile and for single use. While this information is not stated on the labels or in the translated prescribing information, the same applies to the South Korean-authorized product. A sticker or auxiliary label should be generated at pharmacies/hospitals for the outer carton label (and ampoules, if feasible) to ensure proper identification of the product and access to safe use information (including the active ingredient name and strength using mcg/mL). The South Korean-authorized product does not have a Drug Identification Number (DIN) or a barcode that scans in medication management systems in Canada. A facility-generated sticker may be required to enable barcode scanning and allow the product being dispensed and administered to be properly identified. Additional information about South Korean-authorized BONKY Injection, 1 mcg/mL Calcitriol, for reference by healthcare professionals can be found in the English- and French-translated prescribing information at Septa’s Pharmaceuticals Inc. website. Action taken by Health Canada To help mitigate the shortage of Calcitriol Injection USP, 1 mcg/mL in Canada, Health Canada has permitted the exceptional, temporary importation and sale of South Korean-authorized BONKY Injection, 1 mcg/mL Calcitriol and has added this product to the List of Drugs for Exceptional Importation and Sale. Health Canada has worked with Septa Pharmaceuticals Inc. to prepare this alert for South Korean-authorized BONKY Injection, 1 mcg/mL Calcitriol. Health Canada is communicating this important safety information to healthcare professionals and Canadians via the Recalls and Safety Alerts Database on the Healthy Canadians Web Site. This communication update will be further distributed through the MedEffect™ e-Notice email notification system. Report health or safety concerns Managing marketed health product-related side effects depends on healthcare professionals and consumers reporting them. Any case of any serious or unexpected side effects in patients receiving South Korean-authorized BONKY Injection, 1 mcg/mL Calcitriol should be reported to Septa Pharmaceuticals Inc. and/or Health Canada. Septa Pharmaceuticals Inc. 7035 Maxwell Road, Unit 2Mississauga, ONL5S 1R5Canada Telephone: +1 905-564-5665Fax: +1 905-564-1291 To correct your mailing address or fax number, contact Septa Pharmaceuticals Inc. You can report any suspected adverse reactions associated with the use of health products to Health Canada by: • Calling toll-free at 1-866-234-2345; or• Visiting MedEffect Canada's Web page on Adverse Reaction Reporting for information on how to report online, by mail or by fax. For other health product inquiries related to this communication, contact Health Canada at: Regulatory Operations and Enforcement BranchE-mail: [email protected] Telephone: 1-800-267-9675 Devinder KumarPresident & CEOSepta Pharmaceuticals Inc. Appendix 1 Image of South Korean-authorized BONKY Injection, 1 mcg/mL Calcitriol, ampoule and carton: Appendix 2 a) Image of South Korean-authorized BONKY Injection, 1 mcg/mL Calcitriol, outer carton and translation: BONKY Injection, 1 mcg/mL Calcitriol , outer carton: Carton dimension: 145mm (H) x 68mm x 19mm (L) BONKY Injection, 1 mcg/mL Calcitriol , outer carton translation:[Left][분류번호] 311[Classification Code] 311 [원료약품 및 그 분량] 이 약 1mL 중[Composition] Each 1ml contains유효성분 : 칼시트리올(별규).............................................................. 1.0μgActive ingredient : Calcitriol 기타 첨가제 : 무수인산수소나트륨, 아스코르브산나트륨, 에데트산나트륨, 염화나트륨, 인산이수소나트륨일수화물, 주사용수, 폴리소르베이트20Excipients : Sodium hydrogen phosphate anhydrous, sodium ascorbate, sodium edetate, sodium chloride, sodium dihydrogen phosphate monohydrate, water for injection, polysorbate 20 [성상]무색 내지 미황색의 투명한 액이 충진된 갈색 앰플 주사제[Appearance]Colorless to light yellow transparent solution in a brown glass ampoule [효능·효과], [용법·용량], [사용상의 주의사항] 등 자세한 내용은 첨부문서를 참조하십시오. (주의-이상반응)Please refer to the attached document for detailed information on [Indications and Effects], [Dosage and Administration], [Precautions], and other details. (Caution—Adverse Reactions) [저장방법] 차광밀봉용기, 상온보관[Storage] Store in a light-proof, airtight container at room temperature [제조자] 아주약품(주) / 경기도 평택시 산단로 121번길 23[Manufacturer] Aju Pharm Co., Ltd. / 23, Sandan-ro 121beon-gil, Pyeongtaek-si, Gyeonggi-do, Republic of Korea [Right][제조의뢰자] (주)유유제약 / 충북 제천시 바이오밸리1로 94[MAH] Yuyu pharma, Inc. / 94 Bio valley 1-ro, Jecheon-si, Chungcheongbuk-do, Republic of Korea b) Image of South Korean-authorized BONKY Injection, 1 mcg/mL Calcitriol, ampoule label (Original) and translation: Label Dimensions: 20 mm (W) X 31 mm (H) BONKY Injection, 1 mcg/mL Calcitriol, Ampoule Label English translation (Mock-up label)
Dräger VentStar® Resus Neo and VentStar® Resuscitaire
The manufacturer has became aware of cases in which obvious cracks in the hose of the VentStar® Resus Neo and VentStar® Resuscitaire were detected by the users prior to use. In no case draeger was informed of any negative effects on the health of the affected patients. However, this cannot be completely ruled out if such crack remains undetected.
Twins Herbal Products: Undeclared prescription drug (sildenafil)
Products sold without market authorization (DIN) in Canada. Products contain undeclared sildenafil that is listed on the prescription drug list.
Various Godrej Aer Spray recalled due to improper labelling
The recalled products do not meet the labelling requirements of the Consumer Chemicals and Containers Regulations, 2001 under the Canada Consumer Product Safety Act. The lack of appropriate labelling information could result in unintentional exposure to the products and lead to serious illness or injury, including death. As of August 20, 2026, the company has received no reports of incident or injury in Canada.
Maquet Percutaneous Insertion Kit and Dilator Sets
The manufacturer became aware of this issue during retrospective review of historical packaging verification documentation. It was identified that there have been failures in sterile barrier integrity verification testing. As these failures were not previously addressed in accordance with packaging verification requirements, the packaging may not consistently maintain sterile barrier integrity. Therefore, this FSCA is limited to all products of the PIK line within shelf-life.
Allo simonne brand Pistachio Matcha Spread and Almond Cardamom Spread recalled due to pieces of glass
Allo simonne brand Pistachio Matcha Spread and Almond Cardamom Spread recalled due to pieces of glass.
PowerG Walking Pad recalled due to electrical hazard
The affected product does not meet the requirements of the relevant standard for this product category, which poses an electrical hazard. As of August 10, 2026, the company has received no reports of incidents or injuries in Canada.
Hustler or BigDog LED Light Kits and Light Bars recalled due to fire hazard
Under certain unusual operating conditions, temporary voltage surges may cause the LED Light Bars to overheat, posing a fire hazard. As of August 21, 2026, the company has received no reports of incident or injury in Canada or the United States.
Cardinal Health Gynaecology Robotics and Endoscopy Packs
Cardinal Health was recently informed of a medical device recall from Stryker concerning the StrykeFlow PS referenced. the recall is being issued due to an increased amount in reported complaints consistently describing leaking from the handpiece during use.
Apo-Semaglutide Injection : Incorrect dose display
The affected lot may display a 2 mg dose in the dose window and deliver a 2 mg dose instead of the expected 0.25 mg or 0.5 mg dose.
Automated Impella Controller (AIC)
Abiomed has initiated a voluntary medical device recall (removal) after identification of an increase in complaints related to purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly. The cause of the purge flag failures is a combination of dextrose buildup from a purge cassette leak and material embrittlement from usage, aging, or exposure to cleaning chemicals. This issue may occur from usage and is not a manufacturing defect. The purge flag component is present in all manufactured Automated Impella Controller (AIC) in Canada. However, product may continue to be used to ensure continuity of care and a prioritized risk-based strategy for component replacement will be implemented. The purge flag is the component that engages with the purge disc and allows the AIC to recognize the purge disc. These AIC purge flag component failures may result most frequently in user inconvenience due to troubleshooting, attempted purge cassette exchange and AIC exchange. If the failure occurs before initiation of support, exposure may result in a delay to procedure, which is expected to remain clinically manageable in most cases. In the case of an urgent need for mechanical circulatory support or if the failure occurs during active Impella support, exposure may result in a temporary period of inadequate hemodynamic support during controller transition.
Carestation 850
Unexpected shutdown of Carestation 850 and 850C anesthesia systems when AC mains power is disconnected or AC mains power is lost.
Blanketrol® II 115V and Blanketrol® III 115V
Gentherm Medical has received complaints of overheated circuit boards in 0.53% of distributed devices. Overheating can cause the circuit board to stop operating, which may result in a device that shuts down at startup or during use on a patient. Based on the low probability of harm, and absence of reported harm, associated with this issue, users may continue to use the device. In an abundance of caution, it is recommended to have an alternative means of providing therapy available.
Compliments brand Smashed 100% Chicken Burgers recalled due to undeclared egg
Compliments brand Smashed 100% Chicken Burgers recalled due to undeclared egg.
JAMP Temozolomide: Out-of-Specification (Assay)
The active ingredient (temozolomide) is out of specification in the affected lot.
Coaticook brand Aged Cheddar Cheese recalled due to Listeria monocytogenes
The affected products are being recalled from the marketplace due to possible Listeria monocytogenes contamination.
Cuisinart Metal Wire Bristle Grill Brushes recalled due to injury hazard
Small metal wire bristles, from certain Cuisinart-branded metal wire bristle grill brushes, can detach from the brushes and stick to the grill or food, posing an ingestion hazard and risk of serious internal injuries that could require surgery. As of August 26, 2026, the company has received no reports of incidents or injuries in Canada.
BiCOAG Hemostasis Probe
Olympus determined that the affected products may have been manufactured without the designated amount of adhesive to the rear of the device’s ceramic tip, which may result in detachment of the ceramic tip. Customers should immediately discontinue using the BiCOAG Hemostasis Probe products and contact Olympus to return the product.
LEO+ Intracranial Self Expandable Stent And Delivery System
As a precautionary measure, Balt Extrusion is voluntarily recalling specific ANRYV connector lots after routine quality control identified non-conforming bacterial endotoxin test results. The recall affects both standalone ANRYV connectors and ANRYV connectors incorporated into selected Balt product kits, despite no reported patient harm to date.
LIFEPAK ® 35 Monitor/Defibrillator
Stryker has identified an issue with the LP35 where the device does not display the message "CHECK RHYTHM / ECG Analysis Inconclusive" as intended when specific conditions are present simultaneously. The issue does not affect the display of "shock advised" or "no shock advised" messages, and therapy delivery remains available. Additionally, this nonconformance is limited to the device on-screen prompts only; rhythm analysis is not impacted by this issue.
Quantum PureFlow Standard Heat Exchanger High Flow
Blood-to-glycol leakage was identified in the heat exchanger during the procedure. Glycol compartment contamination may result in blood contamination of the heater-cooler due to glycol circulation for thermoregulation. Customer communication is considered necessary to inform users of potential heat exchanger leakage and possible blood contamination of the heater-cooler.
Branch Ergonomic Chairs recalled due to fall hazard
The backrests of the chairs can detach, posing a fall hazard to consumers. As of August 31, 2026, the company has received no reports of incidents or injuries in Canada. In the United States, the company has received 11 reports of backrests detaching from the chairs. No injuries have been reported.
Amana Through the Wall (TTW) air conditioners or heat pumps recalled due to fire hazard
The snubber circuit can emit flames if it shorts, posing a risk of serious injury due to fire hazard. As of September 1, 2026, the company has received no reports of incidents or injuries in Canada. In the United States, the company has received 2 reports of a component on the control board shorting. No injuries have been reported.
DUNLOP RigPro full safety boots recalled due to electric shock hazard
The recalled boots are mislabelled as being static-dissipative when they do not meet those safety certification requirements. The lack of proper electrical shock resistance may not protect users from electrical hazards, posing a risk of an electric shock injury. As of August 26, 2026, the company has received no reports of incident or injury in Canada.
Ten Ten Dim Sum brand buns and dumplings recalled due to undeclared milk
Ten Ten Dim Sum brand buns and dumplings recalled due to undeclared milk.
Cucina d'Oro brand Pesto recalled due to improperly declared cashew
Cucina d'Oro brand Pesto recalled due to improperly declared cashew.
Various pistachios and pistachio-containing products recalled due to Salmonella
The affected products are being recalled from the marketplace due to possible Salmonella contamination.
Imager™ II Angiographic Catheter
Boston Scientific is initiating removal of Imager II Angiographic Catheters (“Catheters”) due to a manufacturing issue affecting the catheter tip. This removal affects the devices identified in Attachment 1 of the customer letter. Boston Scientific has determined that these Catheters were manufactured with reduced levels of stabilizing agents in the tips. This may increase the risk of tip degradation and detachment.
LIFEPAK ® 35 Monitor/Defibrillator
During production of LP35, Stryker identified that certain printer and modem access port connectors may not have been fully seated within the rear housing assembly. As a result, the connectors may appear flush with or recessed relative to the retaining nut rather than extending beyond it as intended.
Spiral Spinning Toy recalled due to choking hazard
The toys contain small balls and are intended for children under three years of age, posing a potential choking hazard. As of September 1, 2026, the company has received no reports of incident or injury in Canada.
Traditional Kohl Products recalled due to chemical hazard
The recalled products contain lead above the impurity limits outlined in the Guidance on Heavy Metal Impurities in Cosmetics. Lead is toxic, especially to children. A range of serious health effects have been associated with exposure to lead, including anemia, vomiting, diarrhea, serious brain injury, convulsions, coma, as well as effects related to the liver, kidneys, heart and immune system. In extreme cases, there have been deaths. Since lead builds up in the body, ongoing exposure to even very small amounts of lead can result in large amounts of lead being present in the body. As of August 28, 2026, the company has received no reports of incident or injury in Canada.
GORE® VIABAHN® Endoprosthesis with PROPATEN Bioactive
Gore has identified through quality control testing that some VIABAHN® devices were processed using equipment that was functioning outside of the validated range. This could potentially result in an incorrect bonding location of the distal tip onto the delivery catheter.
Smarter Snacks brand Vegan Protein Puff Chili & Lime Flavored recalled due to undeclared milk
The affected product is being recalled from the marketplace because it contains milk which is not declared on the label.
Ofood brand Mild Ssamjang Original Seasoned Soybean Paste recalled due to improperly declared peanut
The affected products are being recalled from the marketplace because they contain peanut which is improperly declared on the label.
Woodure Toddler Kitchen Step Stool Model WD1357 recalled due to fall and entrapment hazards
The recalled tower stool model WD 1357 can collapse or tip over while in use, and a child’s torso can fit through the openings on the front and back sides, posing a risk of serious injury and death due to tip over, fall, and entrapment hazards. As of September 6, 2026, the company has received no reports of incidents or injuries from these products in Canada.
Veradius Unity and BV Pulsera Mobile C-Arm System-9in. and 12in. Versions
Air bubbles may develop in the monoblock oil when there is a prolonged period between manufacture and installation, for example due to storage, transportation, or other pre-installation holding time. During a clinical procedure, when the user activates X-ray imaging, if an air bubble becomes trapped in the high-voltage area of the monoblock, there could be an internal electrical discharge (flashover) resulting in X-rays not being generated and consequently no image being displayed on the examination monitor. When this situation occurs, the system displays an error message indicating that the X-ray generator is not available. In some cases, restarting the system (which takes approximately 5 minutes) may restore X-ray generation. Philips' investigation indicates that this issue may occur during the early period of system use following a prolonged period between manufacture and installation. Based on the investigation, potentially affected systems have been identified as those for which more than 300 days elapsed between manufacture and installation and fewer than 250 days have elapsed since installation with continued system use, the monoblock oil temperature increases, allowing storage-related air bubbles to gradually dissipate over time.
Philips Ingenia, Achieva and Intera MR Systems
Philips has become aware of a software issue affecting Philips Magnetic Resonance (MR) imaging systems operating with software versions R5 & R11, which may terminate an examination during the image reconstruction process. If the scan parameters are manually adjusted such that reconstruction requirements exceed the available system memory, the system will freeze, preventing image generation and requiring a system re-start.
Centricity High Acuity Anesthesia
GE Healthcare has become aware of two potential issues associated with certain Centricity High Acuity (CHA) systems. Safety issue #1, involving the order and recording summary component used in displays and printed reports within CHA applications. Safety issue #2, involving the flexible order summary printout component.
Dxc 500i Clinical Analyzer and Dxc 500 AU Clinical Chemistry Analyzer
Beckman Coulter identified a software issue affecting DxC 500i and DxC 500 AU Analyzers when testing plasma samples. Following user configuration of a chemistry test to nondefault units, subsequent activation of a draft configuration in the system configuration page may revert units to the system default without notifying the user.
Generic acetaminophen by Teva recalled because it may contain foreign material
Teva Canada Limited is recalling one lot of the non-prescription drug Novo-Gesic Forte 500 mg (acetaminophen) due to the potential presence of phenolic resin or epoxy which, if ingested, may cause injury to the digestive system. The affected product was supplied to pharmacies in 1,000-count bottles and was dispensed to patients in smaller quantities. Health Canada is monitoring the recall and the company's preventative and corrective actions. If additional safety concerns arise, Health Canada will take appropriate action and inform Canadians as needed.
AGA and La Cornue freestanding dual fuel ranges recalled due to fire hazard
Certain recalled range cookers may be missing a gas manifold testing component. While not required for normal operation, the component is needed during installation pressure testing. If it is missing, gas can leak from the test port when connected to a gas supply, creating a fire hazard. As of August 14, 2026, the company has received no reports of incidents or injuries in Canada or the United States.
IMN Screws System Advanced Locking Screw
Following a product complaint, and as part of its standard quality process, Stryker confirmed that one lot of T2 Alpha IMN advanced locking is incorrectly labeled. The product contains a 75mm length screw instead of 57.5mm.
Olymel brand Chicken Breast Strips recalled due to Listeria monocytogenes
The affected product is being recalled from the marketplace due to possible Listeria monocytogenes contamination.
Goal Zero YETI 3000X Power Stations recalled due to fire and burn hazards
The recalled power station’s circuit board may overheat, posing a risk of fire and burn hazards. As of August 31, 2026, the company has received no reports of incidents or injury in Canada.
Rossdown Farms & Natural Foods brand Meal Starters Black Garlic Chicken Breast products recalled due to undeclared soy
Rossdown Farms & Natural Foods brand Meal Starters Black Garlic Chicken Breast products recalled due to undeclared soy.
PK brand Roasted Lemon N’ Chilli Peanuts recalled due to Salmonella
The food recall warning issued on 2026-09-10 has been updated to correctly identify the code. The correction is marked by an asterisk (*). The affected product is being recalled from the marketplace due to possible Salmonella contamination.