Captus 3000 And 700 (2018-11-04)

Captus 3000 and 700 Recall Summary The Captus 3000 and 700 medical devices have been recalled across Canada. The recall was issued due to a defect or safety concern with the devices themselves. This recall affects all Captus 3000 and 700 devices distributed throughout Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-11-28
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/c25d8c97-62fc-4a46-8edf-3607cb03337f