Biomet Suture Anchors And Retrievers (2016-04-06)

Biomet Suture Anchors and Retrievers Recall Biomet suture anchors and retrievers used in orthopedic surgery are being recalled across Canada. The devices were classified as a Class I recall due to issues identified with the medical devices themselves. This recall affects suture anchors and retrievers that were distributed throughout Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2016-04-29
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/fc34cabc-849f-4457-bc02-f9822e79257e