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

Recall Z-0889-2017 — Covidien Clearify Visualization System Item Code: 21-345 Intended to be used prior to and during endoscopic and laparoscopic procedures to prevent fogging of the scope as well as clean the scope lens

U.S. FDA — Device Enforcement · United States · 2016-10-04 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0889-2017
Date of alert
2016-10-04
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medtronic
Product category
device
Product type
Devices
Reported risk: Product sterility is compromised due to breach of the sterile barrier
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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