—#95534

Product

Zimmer, NexGen Complete Knee Solution LPS Femoral Component, Size F Left, sterile, REF 00-5996-016-01.

FDA product code: JWH — Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Device class: Class 2
Medical specialty: Orthopedic
510(k) numbers: K060370, K960279
Affected lot / code info: 61505607, 61505606, 61495557, 61509649 and 61488058.

Why it was recalled

These lots of Zimmer NexGen Complete Knee Solution LPS Femoral Component and Zimmer NexGen Complete Knee Solution LPS Flex Gender Femoral Component exhibit a nonconforming internal CAM radius. The condition is intermittent and not all devices have nonconforming geometry.

Root cause (FDA determination)

Process design

Action the firm took

The firm sent URGENT DEVICE CORRECTION AND REMOVAL notices to distributors and sales staff, Risk Managers, and implanting surgeons dated 9/15/2010. Sales staff and risk managers were instructed to return any product on hand. Surgeons were informed of the issue but there was no action to be taken by surgeons.

Recalling firm

Firm: Zimmer Inc.
Address: 1800 W Center St, Warsaw, Indiana 46580-2304

Distribution

Distribution pattern: US, Germany, Spain, France, UK, Italy, Sweden, South Africa, Czech Republic, Bulgaria, Poland, Romania, and Austria.

Timeline

Recall initiated: 2010-09-15
Posted by FDA: 2010-12-02
Terminated: 2011-07-27
Status: —

Source: openFDA Device Recall endpoint. Recall record ID #95534. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.