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

Recall Z-2224-2013 — OSTOSTEORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID COBRAID Suture, Blue; Part Number: 72201994 Biodegradable suture anchor

U.S. FDA — Device Enforcement · United States · 2013-08-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2224-2013
Date of alert
2013-08-06
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Smith & Nephew, Inc. Endoscopy Division
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
50261490
Reported risk: Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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