Olympus Corporation of the Americas recalls EVIS EXERA III Gastrointestinal Videoscope
Recalled Product
EVIS EXERA III Gastrointestinal Videoscope
Hazard / Issue
Sterilization failures when devices are sterilized per the Reprocessing Manual due to lack of drying time for the endoscope channel.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Model No. GIF-1TH190; UDI-DI: 04953170343360; All Serial Numbers.
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