Creatine Kinase-mb (ck-mb) (2018-08-05)

Creatine Kinase-MB Recall Summary Creatine kinase-MB (CK-MB) medical devices have been recalled across Canada due to a Class I safety issue. The recall affects CK-MB devices used in medical testing, which measure an enzyme in the blood typically used to help diagnose heart conditions. This is a serious recall classification indicating a potential for significant health impact.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-01-11
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/873fa52e-a08e-4bf9-b9cb-2dba2c3d14fb