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

Recall Z-0581-2019 — Laser Fiber Assy-Single Use-LFS-200-0.22NA-SMA905-Extension Sleeve Silver-Sterile ETO-ForTec Fiber SU-200-TRUE-RT Label Smartscope packaging. The Laser peripherals bare laser fibers, ENT fibers and Endoprobes are intended for use in laser surgical procedure for cutting, coagulating, or vaporiz

U.S. FDA — Device Enforcement · Germany · 2018-10-17 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0581-2019
Date of alert
2018-10-17
Country / jurisdiction
Germany
Risk level
Class II
Risk type
recall
Brand
Leoni Fiber Optics GmbH
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00816901020326
Reported risk: A percentage of the products shipped in Smartscope single-box packaging may exhibit a broken package seal, thus having compromised sterility. There have been two reports of compromised sterility; however, all products packaged in Smartscope single-box packaging are at risk of a compromised product seal. Broken seal pouches compromise sterility and could increase the risk of infection if used.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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