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Olympus Corporation of the Americas recalls EVIS EXERA III Gastrointestinal Videoscope
Recalled November 15, 2023 · FDA recall Z-0288-2024 · Olympus Corporation of the Americas
Hazard
Sterilization failures when devices are sterilized per the Reprocessing Manual due to lack of drying time for the endoscope channel. · FDA Class II
Units
1687 units
Sold at
Nationwide Distribution.
Description
Sterilization failures when devices are sterilized per the Reprocessing Manual due to lack of drying time for the endoscope channel.
Product
EVIS EXERA III Gastrointestinal Videoscope
Manufacturer(s)
Olympus Corporation of the Americas
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →