Hill-Rom recalls CareFusion 303 Inc. Recalls BD Alaris Pump Module Model 8100

Learn more about the CareFusion Recall of the BD Alaris Pump Module

If your email program has trouble displaying this email, view as a webpage. CareFusion 303 Inc. Recalls BD Alaris Pump Module Model 8100 Due to Risk of Stuck or Unresponsive Keys  CareFusion 303 Inc is recalling the BD Alaris Pump Module Model 8100 due to risk of the keypad lifting up from fluid entry. This could lead to keys that become unresponsive or stuck. If this happens, this may lead to serious adverse events, including a delay in patient care or a delay in fluid or medicine delivery through the infusion pump. The FDA has identified this as a Class I recall, the most serious type of recall. Read the Recall Notice Questions? If you have questions, contact the Division of Industry and Consumer Education.

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