Journey Knee System - Femoral Oxinium And Cocr Nonporous Bi-cruciate Stabilized (bcs) (2018-06-19)

Recall Summary Smith & Nephew is recalling certain JOURNEY Knee System femoral components (the thighbone part of the knee implant) made with OXINIUM or COCR materials in the non-porous bi-cruciate stabilized design. The recall is due to a potential manufacturing defect that could affect the implant's performance. This recall affects knee replacements distributed across Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-07-05

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/66d9fa7b-eeed-4bde-b731-d1942938bb7e