Immulite System Progesterone Assays (2017-01-06)

Immulite System Progesterone Assays Recall Siemens Healthcare Diagnostics is recalling Immulite System Progesterone Assays used in clinical laboratories across Canada. The assays may provide inaccurate test results due to a manufacturing issue with certain reagent lots. This recall affects healthcare facilities and laboratories that use this diagnostic testing system.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-01-25

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/bebd74f0-8927-4299-a0e0-ad2e36461bb8