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January 2nd, 2013 | Defective product
January 2, 2013 The U.S. Food and Drug Administration, along with medical device manufacturer, Bunnell, issued a voluntary recall on the Bunnell Life Pulse High-Frequency Ventilator Patient Circuits due to a manufacturing defect. According to an FDA press release, reports have been made of the device overheating and developing electrical fires. The Bunnell Life Pulse High-Frequency… Read More