Visera Imaging System – Hysterovideoscope

Visera Imaging System – Hysterovideoscope Recall The Visera Imaging System Hysterovideoscope is being recalled across Canada because the product may not be sterile. This is a Class I recall, the most serious type, affecting a medical device used in gynecological procedures. The recall applies to all units distributed in Canada.

Product
Visera Imaging System – Hysterovideoscope
Reason
Sterility
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2023-08-04
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/5637af1b-4aa2-4462-b8a6-15dfd462720c