Oes Choledochofiberscopes (2020-08-26)

OES Choledochofiberscopes Recall Summary OES brand choledochofiberscopes (medical devices used to examine bile ducts) are being recalled across Canada due to a device defect. This recall affects healthcare facilities and medical professionals who use these instruments. The recall is classified as Class I, indicating a serious issue with the device.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-09-04
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/ccb1e16a-5e6c-45ef-a6d5-b4c0d79dcae9