Bd Alaris Pump Module Model 8100 (2021-03-03)

BD Alaris Pump Module Model 8100 Recall BD is recalling Alaris Pump Module Model 8100 devices distributed across Canada due to a medical device issue. This is a Class I recall, the most serious classification. The recall affects infusion pump modules used in medical settings.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2021-03-18

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/3bfa447f-cfbf-4a07-b48d-2c710eff9558