Medscape

Voltage Problem Prompts Class 1 Recall of Alaris Pump

CareFusion Corporation has initiated a class 1 recall of the Alaris PC unit model 8015 with software version 9.12 because of a voltage problem, according to the US Food and Drug Administration (FDA).
MD&M East

CareFusion Hit with Another Serious Infusion Pump Recall

FDA has given Class I status to a Carefusion recall related to the Alaris Model 8100 infusion pump. A software failure in the pump had been identified in modules running software version 9.1.18. Last ...
Crain's Detroit

Infusion pump recall has hospitals scrambling whether to replace, repair them

Gift Article 10 Remaining As a subscriber, you have 10 articles to gift each month. Gifting allows recipients to access the article for free. A voluntary safety recall of widely used Alaris infusion ...
Nasdaq

BD Provides Update on Previously Disclosed Recall of BD Alaris System Hardware

FRANKLIN LAKES, N.J., Aug. 20, 2020 /PRNewswire/ -- BD (Becton, Dickinson and Company) (NYSE: BDX), a leading global medical technology company, today provided an update on a previously announced ...