Durepair Dura Subsitute

Durepair Dura Substitute Recall Durepair Dura Substitute, a medical product distributed across Canada, is being recalled because it does not meet sterility requirements. This is a Class I recall, which indicates a serious issue. The product is used as a dura substitute, which is a material placed around the brain and spinal cord during surgery.

Product
Durepair Dura Subsitute
Reason
Sterility
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2023-06-30
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/b9b2f760-c0b3-4f40-84ba-08ee810bddf6