Remel Pathodx Strep Group B Latex (2016-06-15)

REMEL PATHODX STREP GROUP B LATEX Recall Summary REMEL PATHODX Strep Group B Latex test kits are being recalled across Canada because they are medical devices that do not meet required standards. This is a Class I recall, meaning there is a serious potential health risk. The recall affects all units distributed throughout Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2016-07-07
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/d2d79aeb-86ee-4712-84d0-0a5a44a15643