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

Recall Z-0686-2024 — Model No. BF-P190, EVIS EXERA III Bronchovideoscope

U.S. FDA — Device Enforcement · Japan · 2023-12-04 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0686-2024
Date of alert
2023-12-04
Country / jurisdiction
Japan
Risk level
Class II
Risk type
recall
Brand
Shirakawa Olympus Co., Ltd.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
04953170342110
Reported risk: Olympus has updated the instructions for use: Reusable cleaning brushes have been removed from the manual cleaning. Single use brushes remain compatible.
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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