Immulite, 1000 And 2000 System- Progesterone Assay (2019-07-12)

Recall Summary Siemens IMMULITE 1000 and 2000 System Progesterone Assays are being recalled across Canada due to a medical device issue. This product is used in laboratories to measure progesterone levels in patient blood samples. The recall affects all units of this assay that were distributed in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-07-26

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/2a171130-f2a7-4f27-b3f7-cb0cc41fac96