Biodesign® Hiatal Hernia Graft

Biodesign® Hiatal Hernia Graft Recall Summary Biodesign® Hiatal Hernia Grafts are being recalled in Canada due to labelling and packaging issues. This is a Class I recall, which means the product could cause serious health problems or death. The affected grafts were distributed across Canada.

Product
Biodesign® Hiatal Hernia Graft
Reason
Labelling and packaging
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2024-12-19
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/5d74ef86-db28-491e-bb29-3e02e1cbe64c