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FDAJuly 27, 2023device

Olympus Tracheal Intubation Fiberscope, Models LF-P & LF-V.

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

The hazard

Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.

What to do

FDA enforcement status: Ongoing

Brands named

olympus

UPCs

049531700510980495317045293204953170156250

Recall history

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

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