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Manufacturing Deficiencies With Baxter's Infusion Pump

Jamie Sheller

Attorney
(866) 735-1102 Ext 475

Posted by Jamie ShellerJuly 05, 2006 8:40 AM

Tags: Defective Medical Devices

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Baxter Healthcare Corp. (Baxter) has stopped production and distribution of its Colleague Volumetric Infusion Pump and Syndeo Patient Controlled Analgesic Syringe Pump until manufacturing deficiencies are corrected. This action was announced by the FDA and was part of a consent decree signed by Baxter and its CEO and Corporate Vice President. Patients use infusion pumps to control delivery of medication and solutions. Significant problems with some of Baxter's pumps led to FDA inspections and discovery of manufacturing deficiencies.

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Sheller, P.C. (866) 735-1102 Ext 475 www.sheller.com

Jamie Sheller
(866) 735-1102 Ext 475 Email Jamie

Personal Injury Lawyers Serving: Statewide Pennsylvania, Philadelphia, Norristown, Cheltenham, Chester, Drexel Hill, Folsom, Havertown, King of Prussia, Levittown, Radnor, Springfield, Swarthmore, West Chester, Willow Grove

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