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

Recall Z-0309-2020 — Prox Lat Tib Lock Plate and Dist Med Tib Lock Plate Item Nos. 47235700306 47235700308 47235700310 47235700312 47235700314 47235700408 47235700410 47235700412 47235700414 47235700416 47235700504 47235700506 47235700508 47235700510 47235700512 47235700514 47235700518 47235700604 4

U.S. FDA — Device Enforcement · United States · 2019-10-10 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0309-2020
Date of alert
2019-10-10
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Zimmer Biomet, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
47235700306
Reported risk: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
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.

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