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Patient sues Guidant in Minnesota over defective defibrillator
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The Ventak Prizm 2 is one of 11 defibrillator models recalled by Guidant. It's associated with at least 28 malfunctions and one patient death out of 26,000 patients who have the device. (Image courtesy of Guidant Corp.)

The Ventak Prizm 2 is one of 11 defibrillator models recalled by Guidant. It's associated with at least 28 malfunctions and one patient death out of 26,000 patients who have the device.

(Image courtesy of Guidant Corp.)
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