The Alaris PC unit 8015 is part of the Alaris electronic infusion pump that delivers controlled amounts of medications or other fluids to patients through intravenous (IV), intra-arterial (IA ...

The voluntary recall only affects Alaris PC units model 8015 manufactured or serviced between December 2008 and September 2009 and therefore, has no affect on the company's current infusion pump ...

Earlier this month, the FDA had announced a Class I recall of another CareFusion pump, the Alaris PC unit Model 8015, citing a malfunction in its power supply board.

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 ...

This includes system PCs, pump modules and patient-controlled devices for managing pain. A BD Alaris PC Unit (FDA) BD and its CareFusion subsidiary alerted users of potential device errors Feb ...

CHICAGO, July 10 (Reuters) - Carefusion, the medical products business being spun off by Cardinal Health Inc , said it will resume shipments of its Alaris medication infusion pumps. Shipments had ...

San Diego, Calif.-based CareFusion said in July it resumed shipping its Alaris PC pump, whose shipments had been halted because of problems with the product. The company implemented a software ...

In addition to the BD Alaris PC Unit infusion pump, the researchers found patient monitors, cameras, printers, routers, Wi-Fi mesh access points, and a Panasonic door bell camera that are all ...

Researchers at healthcare security firm CyberMDX found two vulnerabilities in the Alaris Gateway Workstation, developed by medical device maker Becton Dickinson. Infusion pumps are one of the most ...

The FDA granted 510(k) clearance to Becton Dickinson’s updated Alaris infusion pump, allowing the company to resume distribution of its system while remediating or replacing older Alaris devices ...

August 23, 2012 — The US Food and Drug Administration (FDA) has notified healthcare providers of a class 1 recall of the CareFusion 303 Alaris Pump Module, Model 8100. In an alert sent yesterday ...

Alaris™ Pump Module Model 8100 In a recall notification sent on April 15, 2019, BD informed clinicians that the bezel assemblies in the Alaris pump modules subject to this recall expansion were ...