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

Recall Z-0154-2021 — OSTEORAPTOR 2.9 W 1UB II BLUE--Absorbable Suture anchor Product Number: 72202165

U.S. FDA — Device Enforcement · United States · 2020-09-09 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0154-2021
Date of alert
2020-09-09
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Smith & Nephew, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
72202165
Reported risk: Product packaging improper or incomplete seal of the pouch surrounding the sterile product may result in a breach of the sterile barrier created by the pouch
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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