Flowtron Acs900 Pump

Flowtron ACS900 Pump Recall Flowtron ACS900 infusion pumps are being recalled because they may deliver incorrect medication doses due to a software defect. The pumps were distributed across Canada and are used to administer drugs to patients. This recall affects healthcare facilities and patients who use this pump model.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-06-21

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/ce48d1d3-d256-4265-9337-ebca4cfdc4ea