Vasoview Hemopro 2 Endoscopic Vessel Harvesting System

Recall Summary The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System is being recalled across Canada due to performance issues. This device is used during surgery to harvest blood vessels for transplant procedures. The FDA has classified this as a Class I recall, which is the most serious level.

Product
Vasoview Hemopro 2 Endoscopic Vessel Harvesting System
Reason
Performance
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2024-06-06
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/c40ab88b-4672-4650-a440-84ca88557ef5