Dvia Diff Timepac 120, 2120i, 2120 (2019-06-28)

Summary Siemens Healthineers is recalling ADVIA DIFF TIMEpac reagent kits used with ADVIA 2120i and 2120 hematology analyzers across Canada. The recall was issued due to a defect in the medical device reagent that could affect test results. This recall affects healthcare facilities and laboratories that use these specific analyzer models.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-07-15
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/c787b449-7431-4b6c-8550-4279ab653736