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Health Canada Medical devices

Evis Exera III Duodenovideoscope

Issued October 10, 2023
Issue
Olympus is initiating this action after becoming aware of recent reports of infections and positive cultures and inquiries from the FDA regarding these reports. Olympus is reminding users to closely follow reprocessing instructions, including periodic inspections by Olympus service, and informing users about an updated manual intended to improve comprehension of existing steps. Olympus is reminding users that the use of a damaged or contaminated endoscope can present an infection risk to patients. Recall start date: le 22 septembre, 2023
Hazard description
Sterility
Product
Product name
Evis Exera III Duodenovideoscope
Reference
ID
RA-74400