Olympus Corporation of the Americas recalls TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP, Model Number:
Recalled Product
TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP, Model Number: LF-GP
Hazard / Issue
Fiberscopes do not have adequate data to support that the suction flow rate meets the device specification.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: UDI-DI: 04953170340215 & UDI-DI: 04953170061998. Serial numbers: 2515143, 2515181, 2515449, 2515549, 2615760, 2615761, 2615763, 2615825, 2615830, 2615831, 2616057, 2616130, 2616199, 2716417, 2817430, 2917855, 2917867, 2917997, 2918003, 2918010, 2918012, 2918030, 2018337, 2018435, 2018486, 2018543, 2018571, 2018675, 2319768, 2319820, 2510582, 2621001.
View official government recall
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