Seeking Alpha

BD Receives FDA 510(k) Clearance for Updated BD Alaris™ Infusion System

This clearance covers updated hardware features for Point-of-Care Unit (PCU), large volume pumps, syringe pumps, patient-controlled analgesia (PCA) pumps, respiratory monitoring and ...
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 ...
Healio

FDA clears updated Alaris infusion pump; recall remediation remains ‘top priority’

Please provide your email address to receive an email when new articles are posted on . The FDA granted 510(k) clearance to Becton Dickinson’s updated Alaris infusion pump, allowing the company to ...
Benzinga.com

Becton Dickinson Recalls Certain Infusion Pumps, Citing Issues With Cardinal Health's Syringes

The FDA has identified this as a Class I recall, the most serious type of recall. There have been 13 reported injuries. There have been no reports of death. Get the Strategy to Trade Pre-Fed Setups ...
Hosted on MSN

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 ...
MD&M East

Alaris, Baxter Run Afoul of FDA with Infusion Pumps

The Syndeo pump could be reintroduced after Baxter fixes its design problems. CDRH has historically been suspicious about the reliability of infusion pumps. Incidents with two pump makers in 2006 have ...
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 ...
Nasdaq

Becton, Dickinson's Alaris Infusion System Gets FDA's 510(k) Clearance

(RTTNews) - Shares of Becton, Dickinson and Company (BDX) gained 5% in the extended trading session on Friday after the medical technology company announced that the updated BD Alaris Infusion System ...
TechCrunch

A widely used infusion pump can be remotely hijacked, say researchers

A workstation used to dock an infusion pump widely used in hospitals and medical facilities has critical security flaws that allow it to be remotely hijacked and controlled, according to security ...
Pharmabiz

BD receives US FDA 510(k) clearance for updated BD Alaris Infusion System

BD (Becton, Dickinson and Company), a leading global medical technology company, announced that the updated BD Alaris Infusion System has received 510(k) clearance from the US Food and Drug ...