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 ...

As the FDA notes, Monoject is one of the most commonly used syringes with infusion pumps and is cited as an example in the Alaris 8015 user manual. The incompatibility problem has prevented the ...

8015, and 8120. These products were distributed between June 19, 2004 and September 22, 2023. The Alaris infusion pump is a modular infusion pump system designed to deliver medications and other ...

CareFusion is recalling 7,418 units of its Alaris Syringe infusion pump, a corrective action that ... including 8000 and 8015, which recalled in December 2013 because they produced audible alarms ...

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 ...

The Alaris pumps are used to deliver preset amounts of medications, nutrients and other fluids to patients via IV. The identified vulnerabilities affect Alaris systems equipped with Guardrails ...

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 ...