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

Recall Z-2577-2017 — Por fullct fem st 15x200mm, Sterile, prosthesis, hip, semi-constrained, metal/polymer, porous uncemented- Specific Knee, Hip and Nail Implants

U.S. FDA — Device Enforcement · United States · 2017-02-28 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2577-2017
Date of alert
2017-02-28
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Zimmer Biomet, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00784301508
Reported risk: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for sterile-packaged implants packaged in two different package configurations due to packaging design verification test failures.
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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