Olympus Endoscope Reprocessor

Olympus Endoscope Reprocessor Recall Olympus Endoscope Reprocessors are being recalled in Canada because they may not properly sterilize endoscopes, which could allow bacteria or other harmful microorganisms to remain on medical equipment used during patient procedures. This is classified as a Class I recall, the most serious type. The affected products were distributed across Canada.

Product
Olympus Endoscope Reprocessor
Reason
Sterility
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2024-02-08
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/05c0f4c1-b68c-41d4-9de0-15adb2d5254b