Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
POROUS PATELLA 32MM X 10MM - 00587806532 POROUS PATELLA 35MM Recalled by Zimmer Trabecular Metal Technology, Inc. Due to Zimmer Biomet is initiating a recall of specific...
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 Trabecular Metal Technology, Inc. directly.
Affected Products
POROUS PATELLA 32MM X 10MM - 00587806532 POROUS PATELLA 35MM X 10MM- 00587806535 POROUS PATELLA 38MM X 10MM - 00587806538 POROUS PATELLA 41MM X 10MM - 00587806541
Quantity: 19,884 total
Why Was This Recalled?
Zimmer Biomet is initiating a recall of specific lots of foil pouched, sterile Trabecular Metal implants that were manufactured between April 2011 and October 2012. The foil pouches are part of a dual barrier system to provide sterile integrity.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Zimmer Trabecular Metal Technology, Inc.
Zimmer Trabecular Metal Technology, Inc. has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report