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

Olympus Corporation of the Americas: Olympus Bronchovideoscope, Models BF-1T150, BF-1T60, BF-MP60, BF-P150, BF-P60, BF-PE2, BF-TE2, BF-XT160.

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: 1715 units Lot/code info: UDI-DI: 04953170308185, 04953170288968, 04953170308161, 04953170339264, 04953170308277, 04953170339394, 04953170308178, 04953170288876, 04953170308123, 04953170339196, 04953170062988, 04953170339974, 04953170063008, 04953170339998, & 04953170340147; All Serial Numbers.

UPC codes

04953170308185, 04953170288968, 04953170308161, 04953170339264, 04953170308277, 04953170339394, 04953170308178, 04953170288876, 04953170308123, 04953170339196, 04953170062988, 04953170339974, 04953170063008, 04953170339998, 04953170340147

Source

Official record: FDA (Device enforcement)

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

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