Optilite Igm Kit (2019-07-19)

Optilite IgM Kit Recall Summary The Optilite IgM Kit, a medical diagnostic device, has been recalled across Canada due to safety or effectiveness concerns that warrant a Class I classification. The recall affects all units of this product that were distributed throughout Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-08-16
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/628ac216-0fdf-41e4-8277-30f6b474bd57