CareFusion 303, Inc. Recalls BD Alaris Pump Module Model 8100 Due to Risk of Stuck or Unresponsive Keys

Date: 04/16/21

BD Alaris Infusion Pump Module

• Affected Model Number: 8100
• Affected Parts: 49000239; 49000346; 49000438; 49000439
• Manufacturing Dates: 01/15/2019 to 12/05/2019.
• Distribution Dates: January 23, 2019 to December 5, 2019
• Devices Recalled in the U.S.: 145,492
• Date Initiated by Firm: March 3, 2021

USA-FDA Link: https://www.fda.gov/medical-devices/medical-device-recalls/carefusion-303-inc-recalls-bd-alaris-pump-module-model-8100-due-risk-stuck-or-unresponsive-keys