Rchitect I System - Estradiol Assay (2016-03-30)

Architect I System - Estradiol Assay Recall The Architect I System Estradiol Assay, a medical device used to measure estradiol levels in blood samples, has been recalled across Canada. The recall was issued on March 30, 2016, and classified as Class I, indicating a serious issue. This device is used in hospitals and diagnostic laboratories that operate Architect I analyzers.

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/e5db0e08-79d8-47a9-be3d-4527e24a0b62