Ctive Amh Gen II Elisa

Recall Summary Active AMH Gen II Elisa test kits are being recalled across Canada due to a quality issue with the product. This is a Class I recall, which means the product could cause serious health problems or death. The recall affects this diagnostic test kit used in medical settings.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2013-01-07

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/1df24950-1dfb-4b8c-b889-9367900960d9