Vidas System - Toxo Igm (txm) Assay (2016-02-08)

Recall Summary The VIDAS SYSTEM - TOXO IGM (TXM) ASSAY, a medical device used to test for toxoplasmosis infection, has been recalled across Canada. The device was recalled due to issues that classify it as a Class I recall, the most serious type. This recall affects all Canadian users of this particular assay test.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2016-04-07
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/99d50615-ac19-41fc-87e7-0fda9e558cd7