Product RecallProduct RecallHighRecall Date: Sep 4, 2026
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.
- Status
- Active
- Key date
- Sep 4, 2026
- Provinces
- National
- Added
- Sep 4, 2026
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