Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2566-2014 — Biomet Microfixation Temporomandibular Joint (TMJ) Patient Matched Left Fossa Part# CP751506 The Total Temporomandibular Joint (TMJ) replacement system is implanted in the jaw to functionally reconstruct a diseased and/or damaged temporomandibular joint. The Total TMJ replacement system is a two

U.S. FDA — Device Enforcement · United States · 2013-09-20 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2566-2014
Date of alert: 2013-09-20
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Biomet Microfixation, LLC
Product category: device
Product type: Devices

Reported risk: Product mix occurred prior to final package and labeling process.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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