Vidas Toxo Igg Avidity (2016-08-09)

VIDAS TOXO IGG AVIDITY Recall Summary The VIDAS TOXO IGG AVIDITY medical device has been recalled across Canada due to a Class I safety issue. This device is used for blood testing to detect toxoplasmosis infection and assess immunity. The 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

2016-08-26

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/443521ae-4e1f-475a-9c7a-bfeafbf8545e