Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Lateral Troch Plate Full Crimp - 254mm Recalled by Zimmer Biomet, Inc. Due to Possibility that the patient label inside the product...
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 Biomet, Inc. directly.
Affected Products
Lateral Troch Plate Full Crimp - 254mm, model # 350838
Quantity: N/A
Why Was This Recalled?
Possibility that the patient label inside the product box was incorrectly labeled. The outer box label and actual product are correctly identified but the internal patient label could be incorrect.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Zimmer Biomet, Inc.
Zimmer Biomet, Inc. has 875 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report