BD Alaris Infusion Pump Module Model 8100 Recalled Again and Labeled Class I Event by FDA WASHINGTON, DC - The US Food and Drug Administration announced that BD / CareFusion 303 Inc is recalling 145,000 of its Becton Dickinson Alaris pumps.  The recall is classified as a Class I recall because the pump's defect may cause serious … [Read more...] about BD Alaris Infusion Pump Module Model 8100 Recall