Baxter Healthcare Corp. recalled all models of its Colleague Volumetric Infusion Pumps because the pumps can shut down while delivering medication and fluids to patients, the Food and Drug Administration said. Approximately 255,000 of the pumps are in use, including 206,000 in the U.S., but users should not at this time return the pumps to Baxter, the FDA said. The agency deemed it a Class I recall, the most serious type. Baxter received six reports of serious injury and three reports of deaths associated with the problem, the FDA said. The company has stopped shipping the pumps until the problems are resolved. In March, Baxter advised customers to stop using pumps that exhibited specific failure codes and have the pumps inspected by authorized service personnel. -- by Cinda Becker
Baxter recalls flawed infusion pump after deaths
Send us a letter
Have an opinion about this story? Click here to submit a Letter to the Editor, and we may publish it in print.
Recommended for You