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: Portland Personal Injury LawyerCertain Models of Triple-Channel Infusion Pumps Recalled
By Jenny Albano
On Friday, the FDA alerted healthcare professionals of a class 1 recall of certain models of an upgraded triple-channel volumetric infusion pump made by Colleague and Colleague CX. A software malfunction may sound an alarm in the device, showing an error code 16:310:867:0002, which will stop infusing.
An electronic infusion pump delivers controlled amounts of medicine or other fluids to patients through a direct line into the bloodstream (intravenously, intra-arterially, or through an epidural).
Full post as published by Portland Personal Injury Lawyer on July 25, 2007 (boomark / email).
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