Zymutest Hia Iggam Monostrip (2018-02-06)

ZYMUTEST HIA IgGAM MonoStrip Recall The ZYMUTEST HIA IgGAM MonoStrip, a medical device used for testing, is being recalled across Canada. The recall was issued on February 6, 2018, and is classified as Class I, which indicates a serious issue. This recall affects all units of this product distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-03-23
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/3b8ccced-e691-432f-864e-d91f8eb59035