CareFusion 303, Alaris Pump Module, Model 8100: Class I Recall – potential for pump malfunction to stop infusion

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Intravenous news: The FDA report “FDA notified healthcare professionals of a Class I Recall of the CareFusion 303, Alaris Pump Module, Model 8100, due to a potential for the pump module door keypad overlay to become loose, peel away, or separate from the door assembly. This could cause a potential for fluid ingress which could lead to a keypad malfunction, causing the infusion to stop with alarm. When infusion stops, serious injury or death may result.”

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