Bd Alaris Pump Module Model 8100 (2020-08-05)

BD Alaris Pump Module Model 8100 Recall BD is recalling the Alaris Pump Module Model 8100 across Canada because of a problem with the medical device itself. This is a Class I recall, which means the device could cause serious harm or death. The recall affects all Alaris Pump Module Model 8100 units that were distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-08-28
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/dc29df93-3a8c-4d81-b2c3-4471d3c4bbab