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FDAJune 8, 2023device

Olympus BRONCHOFIBERSCOPE BF Type, Model Numbers BF-PE2, BF-TE2

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

0495317033997404953170339998

Recall history

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

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Olympus BRONCHOFIBERSCOPE BF Type, Model Numbers BF-PE2, BF-TE2 — Recall Details · AllClear