Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Biomet Parsippany Recalled by Biomet Spine, LLC Due to Mislabeling
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 Biomet Spine, LLC directly.
Affected Products
Biomet Parsippany, NJ. 4 0 MM X 14 MM Variable Screw C-Tek Maxan Anterior Cervical Plate System. Lot 375440.
Quantity: 7 parts
Why Was This Recalled?
Some of P/N 14-521614B Lot 375440 was mislabeled as P/N 14-521614 Lot 375440.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Biomet Spine, LLC
Biomet Spine, LLC has 13 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report