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.
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