Remipack (2018-03-28)

Remipack Recall Summary Remipack medical devices are being recalled in Canada due to a safety issue. The recall applies to all Remipack devices distributed across Canada. This is classified as a Class I recall, which is the most serious type.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-04-06
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/b73f9fbd-bc69-436f-adb1-998f883bee4f