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

Recall Z-1006-2019 — NexGenTrabecular Metal Tibial Half Block Augment, Left Lateral/Right Medial, Size 4 5MM Thickness W/Screws Item Number: 00544800436 Product Usage: The Trabecular Metal Tibial Cone Augments are intended for use where severe degeneration, trauma, or other pathology of the knee joint indicates to

U.S. FDA — Device Enforcement · United States · 2019-02-01 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1006-2019
Date of alert: 2019-02-01
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Zimmer Trabecular Metal Technology, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 63244259

Reported risk: Potentially comingled, resulting in the product in the box potentially not matching the product on the label

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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