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

by FDA on August 22, 2012

in MedWatch

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

This is a summary of an alert issued by MedWatch: The FDA Safety Information and Adverse Event Reporting Program. The link below will take you to the original notice.

View Full Details Of The Original MedWatch Notice Here.

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