Zimmer M/l Taper Taperfemoral Stem

Zimmer M/L Taper Taperfemoral Stem Recall Zimmer is recalling M/L Taper Taperfemoral Stem devices across Canada due to labelling and packaging issues. This is a Class I recall, the most serious classification. The recall affects hip replacement stem devices that were distributed throughout Canada.

Product
Zimmer M/L Taper Taperfemoral Stem
Reason
Labelling and packaging
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2023-08-17
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/b9712eb5-99e5-4c6f-8597-81d01d078f2d