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FDA (Device enforcement)Recalled 2023-07-27class ii

Olympus Corporation of the Americas: Olympus Bronchovideoscope, Models BF-1T180, BF-1TQ180, BF-P180, & BF-Q180.

Hazard

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

Details from the source

Reason for recall: Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large. Distribution: US Nationwide distribution. Quantity: 3652 units Lot/code info: UDI-DI: 04953170308215, 04953170288975, 04953170339325, 04953170308222, 04953170289002, 04953170339349, 04953170308192, 04953170317965, 04953170339288, 04953170288883, 04953170308208, 04953170288937; All Serial Numbers.

UPC codes

04953170308215, 04953170288975, 04953170339325, 04953170308222, 04953170289002, 04953170339349, 04953170308192, 04953170317965, 04953170339288, 04953170288883, 04953170308208, 04953170288937

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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