Linity C & I Processing Module (2019-09-19)

Alinity C & I Processing Module Recall Summary Abbott is recalling the Alinity C & I Processing Module devices distributed across Canada due to a medical device issue. The FDA classified this as a Class I recall, which is the most serious category. The recall affects processing modules used in laboratory equipment that were distributed nationwide in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-11-15
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/bf3671c3-58c1-451c-8d7c-aa07f608e588