CareFusion 303, Alaris Pump Module, Model 8100: Class I Recall – Potential for Pump Malfunction To Stop Infusion

by admin on August 26, 2012

A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: CareFusion 303, Alaris Pump Module, Model 8100: Class I Recall – Potential for Pump Malfunction To Stop Infusion. According to the Food & Drug Administration FDA’s MedWatch:

Risk of the pump module door keypad overlay to separate from the keypad assembly, which could lead to a keypad malfunction.

For more information on the drug or medical device recall or safety alert, read the Food & Drug Administration’s FDA’s drug or medical device recall or safety alert: CareFusion 303, Alaris Pump Module, Model 8100: Class I Recall – Potential for Pump Malfunction To Stop Infusion.

To report an adverse reaction, problem or other issue with a drug or medical device, submit a drug or medical device complaint to the government at fda.gov or MedWatch.

If you have thoughts on the drug or medical device recall or safety alert, share your drug or medical device recall or safety alert comments below.

Share Your Recall Comments Below!

    What Do You Think? Share Your Recall Comments!

    Previous post:

    Next post: