Utoimmune Eia Anti-tissue Transglutaminase (ttg) Iga (2019-04-10)

Recall Summary Autoimmune EIA Anti-Tissue Transglutaminase (tTG) IgA test kits are being recalled across Canada. These medical devices are used to detect antibodies related to celiac disease and other autoimmune conditions. The recall affects healthcare providers and laboratories that use this diagnostic test.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-05-10

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/8de89e37-9600-49e9-ba02-be6137942c05