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

Recall Z-2490-2023 — Olympus Bronchovideoscope, Models BF-1T150, BF-1T60, BF-MP60, BF-P150, BF-P60, BF-PE2, BF-TE2, BF-XT160.

U.S. FDA — Device Enforcement · United States · 2023-07-27 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2490-2023
Date of alert
2023-07-27
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)
04953170308185
Reported risk: Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
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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