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

Recall Z-0192-2024 — EVIS EXERA III BRONCHOVIDEOSCOPE Model Numbers BF-1TH190, BF-H190, BF-Q190 and BRONCHOVIDEOSCOPE OLYMPUS BF-Q170 Model Number BF-Q170

U.S. FDA — Device Enforcement · United States · 2023-10-12 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0192-2024
Date of alert
2023-10-12
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Olympus Corporation of the Americas
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
4953170335181
Reported risk: There is a risk of endobronchial combustion if high-frequency cauterization is performed while supplying oxygen [and/or] the electrode section of the electrosurgical accessory is too close to the distal end of the endoscope.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.