Baxter Infusion Pump Recall: Pump Failure Could Result in Death
-AboutLawsuits
03/13/2009 - Baxter Colleague Infusion pumps, which are widely used at hospitals throughout the United States to deliver IV fluids and medicine, have been recalled by the FDA because the devices could delay or interrupt the infusion of fluids, potentially resulting in serious personal injury or death. More>>>
Baxter's Colleague infusion pump under FDA's most serious recall
-ChicagoTribune
03/13/2009 - Baxter International Inc. disclosed Wednesday that the latest flaw it identified with its frequently problem-plagued Colleague infusion pump has been classified by the Food and Drug Administration as a "Class 1 recall," the regulatory agency's most serious recall designation. More>>>
Recall Issued on Baxter Electronic Infusion Pumps
-Medscape
03/12/2009 - A class 1 recall has been issued on Baxter Healthcare Corp Colleague Single and Triple Channel Volumetric Infusion Pumps manufactured and distributed between February 1997 and December 2008, the US Food and Drug Administration (FDA) says. More>>>
If you or a loved one suffered injuries or death from a recalled Baxter COLLEAGUE or Flo Guard Volumetric infusion pump you may be entitled to compensation. Contact the Baxter infusion pump attorneys of Ennis & Ennis, P.A. today by filling out our free case evaluation form on this page or by calling toll-free 1-800-856-6405. Our experienced lawyers can answer any questions you may have about the Baxter infusion pump recall and potential Baxter infusion pump class action lawsuit.
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