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

Recall Z-2737-2014 — Persona The Personalized Knee System 2.5 mm Female Screw 48 mm Length Sterile Qty-2. Sterilized using irradiation, single use.

U.S. FDA — Device Enforcement · United States · 2014-09-09 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2737-2014
Date of alert
2014-09-09
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Zimmer, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
62155015
Reported risk: The Persona 48mm X 2.5mm Female Screw is being recalled due to potential use of the screw in cortical bone, and corresponding stripping of the 2.5mm Persona Hex Driver.
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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