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

Recall Z-1239-2017 — Smith & Nephew Dyonics Saw Blade, Standard, Product Number 3701

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

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1239-2017
Date of alert
2017-02-02
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Smith & Nephew, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
50586138
Reported risk: The single use devices are provided sterile and do not have an expiration date on the label.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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