Product Wiki · Recalls · Health Canada — Medical Devices

Duramatrix-Onlay ® Collagen Dura Substitute Membrane — recall 63806

Health Canada — Medical Devices · Canada · 2022-01-10 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
63806
Date of alert
2022-01-10
Country / jurisdiction
Canada
Authority classification
Type II
Notice type
recall
Product category
General and plastic surgery
Product type
Medical devices
Reported risk: The outer pouch packaging of the product may not be sealed. The product is provided sterile within an inner pouch, which is placed within an outer pouch. A single unit of another product from the same lot was found with an open seal during final packaging on December 1, 2021. Recall start date: Dec 6, 2021
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/duramatrix-onlay-r-collagen-du

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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