Archived - Important Medical Devices Safety Advisory - Tutoplast Dura Manufactured By Tutogen Medical Gmbh

Recall Summary Tutoplast Dura, a surgical membrane manufactured by Tutogen Medical GmbH, has been recalled across Canada. The recall was issued due to safety concerns with the product, though the specific reason is not detailed in the provided information. The product was distributed to healthcare facilities and hospitals throughout Canada.

Category

drug recall

Country

Canada

Agency

HC-DRUGS

Recall date

2002-04-11

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DRUGS

Recall details on Nibble Recalls: https://trynibble.app/recalls/ca9c42c4-5ad6-4f06-b3f4-ea330979f50f