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.
130 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.
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.
Lancora Tablets; Broken / partial tablets in blister pack
Presence of partial tablets in the blister packs.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
JAMP Chlorthalidone 12.5 mg tablet: Out of specification (Dissolution)
The dissolution may be out of specification in the affected lot.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
StrykeFlow PS and AHTO
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
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.
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.
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.
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
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.
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.
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.
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.
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.
Briine brand Pacific Tide Sparkling Spring Water recalled due to bulging cans
Briine brand Pacific Tide Sparkling Spring Water recalled due to bulging cans.
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.
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.
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.
Izem Energy brand energy drinks recalled due to labelling issues
Izem Energy brand energy drinks recalled due to labelling issues.
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.
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.
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.
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.