Transpac Monitoring Kits (2016-09-27)

Recall Summary Transpac Monitoring Kits have been recalled across Canada due to issues with the medical device. This is classified as a Class I recall, which is the most serious type. The kits were distributed throughout Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2016-09-27
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/0556876c-5764-473e-9742-f00899933395