Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
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.
04953170308185, 04953170288968, 04953170308161, 04953170339264, 04953170308277, 04953170339394, 04953170308178, 04953170288876, 04953170308123, 04953170339196, 04953170062988, 04953170339974, 04953170063008, 04953170339998, 04953170340147
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.