Laris System- Syringe Pump Module Model 8110 Software Versions 9.15 And 10.5

Recall Summary Baxter is recalling the Alaris System Syringe Pump Module Model 8110 with software versions 9.15 and 10.5 due to a software issue that could cause the pump to stop delivering medication without alerting users. This recall affects healthcare facilities across Canada that use these specific pump models and software versions.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-08-12

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/54fb230d-8d37-4bc9-b4b0-9d00c0101101