Monthly Prescribing Reference

Compatibility Issues Prompt Recall of Alaris Infusion Pumps

To data, there have been 13 reported injuries. Becton Dickinson (BD)/Carefusion 303 is recalling the Alaris infusion pump due to incompatibility issues with Cardinal Health Monoject syringes. The Food ...
FierceBiotech

FDA designates BD's wide-ranging Alaris infusion pump recall as Class I

BD is recalling hundreds of thousands of its Alaris infusion pumps and vital sign monitors due to multiple system faults, including software- and user-related issues. According to the FDA, the errors ...
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 ...
FierceBiotech

CareFusion recalls its Alaris infusion pump, the franchise's 9th Class 1 recall since 2010

CareFusion is recalling 7,418 units of its Alaris Syringe infusion pump, a corrective action that the FDA just deemed Class 1. This marks CareFusion's ninth Class 1 recall of an Alaris device since ...
Seeking Alpha

BD expands recall of its Alaris Pump Module model 8100

The U.S. FDA said that BD (NYSE:BDX) has expanded its Class I voluntary recall to inform customers about the worst-case performance of the BD Alaris Pump Module model 8100 when used with certain ...
Reuters

FDA Says Becton Dickinson Carefusion 303 Recalls Alaris System Infusion Pumps Due To Software, System Errors

* FDA SAYS BD/CAREFUSION 303 RECALLING ALARIS INFUSION PUMP SYSTEM & MODULES DUE TO MANY SYSTEM ERRORS WHICH HAVE CAUSED 55 REPORTED INJURIES, 1 DEATH * FDA- ON FEB 4, BD/CAREFUSION 303 SENT LETTERS ...