CORRECTION – 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. Note: The subject line of the email sent earlier today incorrectly identified Hill-Rom, rather than CareFusion 303 Inc., as the firm recalling the device. This has been corrected in the subject line of this email.  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

Follow us on Twitter at @FDADeviceInfo Manage Subscriptions  |  Unsubscribe All  |  Help

This email was sent to ooseims.archieves@blogger.com using GovDelivery Communications Cloud on behalf of: U.S. Food and Drug Administration ·  10903 New Hampshire Ave · Silver Spring, MD ·  20993-0002 ·  1-888-INFO-FDA