OFFICIAL-SOURCE RECALL · CANADA
GORE® VIABAHN® Endoprosthesis with PROPATEN Bioactive Recall: Gore has identified through quality control
Use the identifiers printed on your item to determine whether this recall may affect the product you own.
CHECK THE ITEM YOU OWN
Is your product affected?
- Brand
- See official notice
- Product
- GORE® VIABAHN® Endoprosthesis with PROPATEN Bioactive
- Manufacturer
- See official notice
The barcode may identify the product type, while the recall may apply only to certain lots, dates or variants. Check all identifiers listed in the official recall.
Why this product was recalled
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.
Hazard
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.
Official recall notice
GORE® VIABAHN® Endoprosthesis with PROPATEN Bioactive
Agency: Health Canada
Official publication date: October 7, 2026
Read the official CANADA_HEALTH recall notice →SCAN ONCE. KEEP WATCHING.
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