Procarve Foot Standard And Firm And Knee Join

Recall Summary Procarve Foot Standard, Procarve Foot Firm, and Procarve Knee Joint medical devices are being recalled across Canada. The devices are being recalled due to issues related to their classification as medical devices. This recall applies to all Procarve Foot and Knee Joint products distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2016-09-16
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/7c92b0de-443b-42bb-aa9c-7fa965a6a7f6