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: 3652 units Lot/code info: UDI-DI: 04953170308215, 04953170288975, 04953170339325, 04953170308222, 04953170289002, 04953170339349, 04953170308192, 04953170317965, 04953170339288, 04953170288883, 04953170308208, 04953170288937; All Serial Numbers.
04953170308215, 04953170288975, 04953170339325, 04953170308222, 04953170289002, 04953170339349, 04953170308192, 04953170317965, 04953170339288, 04953170288883, 04953170308208, 04953170288937
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.