Biodesign® Fistula Plug

Biodesign® Fistula Plug Recall The Biodesign® Fistula Plug is being recalled across Canada due to issues with its labelling and packaging. This is a Class I recall, the most serious classification. The product is distributed throughout Canada.

Product
Biodesign® Fistula Plug
Reason
Labelling and packaging
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2024-08-21
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/60536774-629e-4348-8ec1-4dce8e7fe7b3