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

Recall Z-1132-2023 — EVIS EXERA III Colonovideoscope-For endoscopy and endoscopic surgery within the lower digestive tract (including the anus, rectum, sigmoid colon, colon, and ileocecal valve) Model/Serial: CF-Q180AL

U.S. FDA — Device Enforcement · United States · 2022-12-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1132-2023
Date of alert
2022-12-21
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Olympus Corporation of the Americas
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
04953170202315
Reported risk: A single CF-Q180AL colonovideoscope was utilized in a veterinary endoscopy procedure in advance of being assigned to a medical facility as a service loaner in error, potential for microbial contamination
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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