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FDAJuly 27, 2023device

Olympus Tracheal Intubation Fiberscope, Models LF-DP, LF-GP, & LF-TP.

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

049531701368560495317034019204953170061998049531703402150495317031757604953170136825

Recall history

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

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Olympus Tracheal Intubation Fiberscope, Models LF-DP, LF-GP, & LF-TP. — Recall Details · AllClear