Olympus Corporation of the Americas recalls Olympus Tracheal Intubation Fiberscope, Models LF-DP, LF-GP,
Recalled Product
Olympus Tracheal Intubation Fiberscope, Models LF-DP, LF-GP, & LF-TP.
Hazard / Issue
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: UDI-DI: 04953170136856, 04953170340192, 04953170061998, 04953170340215, 04953170317576, & 04953170136825; All Serial Numbers.
View official government recall
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