MedTech Dive

FDA flags risk from dropped BD Alaris pumps after 2 injury reports

BD has written to users of its Alaris pump modules about a risk associated with two complaints of serious injury. The Food and Drug Administration, which shared details of the letter Friday, has ...
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).
Yahoo Finance

BD tells customers not to use Cardinal’s Monoject syringes with Alaris pumps

The Food and Drug Administration has posted a Class I notice about Becton Dickinson infusion pumps affected by compatibility issues with Cardinal Health Monoject syringes. Cardinal sent an urgent ...
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 ...
Medscape

Recall of Alaris Infusion Pump Computer Component

The US Food and Drug Administration (FDA) has notified healthcare providers of a class 1 recall of CareFusion's Alaris PC unit (model 8015) with software version 9.12. The Alaris PC unit is the ...
CNN

BD Hits Century Mark With Infusion Pump Interoperability

FRANKLIN LAKES, N.J., July 19, 2016 /PRNewswire/ -- BD (Becton, Dickinson and Company) (NYSE: BDX), a leading global medical technology company, today announced that more than 100 hospitals and health ...
Morningstar

Duncan Regional Hospital Becomes First in U.S. to Implement BD Alaris™ EMR Infusion Interoperability with MEDITECH

FRANKLIN LAKES, N.J., Nov. 13, 2025 /PRNewswire/ -- BD (Becton, Dickinson and Company) (NYSE: BDX), a leading global medical technology company, today announced that Duncan Regional Hospital ("DRH ...