Immulite & 1000 & 2000 System - Acth Assay (2020-03-27)

Recall Summary Siemens is recalling IMMULITE & 1000 & 2000 System ACTH Assay kits used to measure adrenocorticotropic hormone (ACTH) levels in patient blood samples. The kits were recalled due to a manufacturing issue that could affect test accuracy. The affected products were distributed across Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2020-04-17

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/f6dd2b58-47d4-46a4-9483-f71930e187fd