Bioplex 2200 Ana Screen Control Set (2019-11-06)

BioPlex 2200 ANA Screen Control Set Recall The BioPlex 2200 ANA Screen Control Set, a medical device used in laboratory testing, has been recalled across Canada. The recall was issued due to concerns with the device itself. This recall affects all locations in Canada that use this product.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-11-29
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/c150c07e-ebe3-4bb0-a7e1-c0b6da41a9ef