Bx Pentra 400 Clinical Chemistry System (2016-02-19)

ABX PENTRA 400 Clinical Chemistry System Recall The ABX PENTRA 400 Clinical Chemistry System, a laboratory device used for blood testing, has been recalled across Canada. The recall was issued due to a problem with the medical device itself, though specific details about the defect are not provided in this notice. This recall affects clinical laboratories and healthcare facilities that use this equipment.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2016-05-31
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/83a42480-af19-4952-8051-222756aea530