Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Zimmer¿ Unicompartmental Knee Femoral Component. Indicated for patients with painful Recalled by Zimmer, Inc. Due to The low density polyethylene (LDPE) bag used to...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Zimmer, Inc. directly.
Affected Products
Zimmer¿ Unicompartmental Knee Femoral Component. Indicated for patients with painful and/or disabling knee joint.
Quantity: 32537
Why Was This Recalled?
The low density polyethylene (LDPE) bag used to package implants adheres to the highly polished surface of the devices.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Zimmer, Inc.
Zimmer, Inc. has 437 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report