Ramp Liquid Cardiac Controls Product (2019-03-13)

Recall Summary RAMP Liquid Cardiac Controls, a medical device product, has been recalled across Canada due to quality or safety issues. This Class I recall indicates a serious problem with the product. The recall affects all Canadian consumers and healthcare facilities that have this cardiac control product.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-04-29
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/2489e18c-897a-4a62-9d8f-42159ff409fe