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

Recall Z-2603-2014 — CLAW II 2 HOLE PLATE ORTHOLOC 3DSi, LENGTH 25mm, REF 40240225, 1 EACH, Rx ONLY, NON STERILE Orthopedic

U.S. FDA — Device Enforcement · United States · 2014-07-30 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2603-2014
Date of alert
2014-07-30
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Wright Medical Technology, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
40240225
Reported risk: Plates manufactured from an incorrect raw material.
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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