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FDAJune 8, 2023device

Olympus EVIS EXERA BRONCHOVIDEOSCOPE BF TYPE, Model Number BF-XT160

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.

What to do

FDA enforcement status: Ongoing

Brands named

olympus

UPCs

04953170340147

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Olympus EVIS EXERA BRONCHOVIDEOSCOPE BF TYPE, Model Number BF-XT160 — Recall Details · AllClear