Bellavista 1000, Bellavista 1000(neo) & Bellavista 1000e (2019-10-30)

Recall Summary Bellavista 1000, Bellavista 1000 (Neo), and Bellavista 1000E medical devices are being recalled across Canada due to safety or effectiveness concerns. This is a Class I recall, indicating a serious issue with the devices. The recall affects all units of these devices that were distributed throughout Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-11-26
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/54095a23-4a71-48a1-bf89-124ffd5507be