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Guidant Defibrillators
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Which Guidant cardiac defibrillator was implanted?

If other, what is the name of the defibrillator that was implanted?

Date the device was implanted:

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What medical condition prompted the use of the device?

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Guidant contractor gets subpoena about devices

Nov 22, 2005 | St. Paul Pioneer Press Accellent Inc., a contract manufacturer for heart-device makers including Guidant Corp., said it received a U.S. Justice Department subpoena for information related to a probe of Guidant defibrillators.

The subpoena is connected to an investigation by the U.S. Attorney's office in Minneapolis that last month prompted a separate subpoena to Guidant, Wilmington, Mass.-based Accellent subsidiary, Accellent Corp., said Monday in a filing with the U.S. Securities and Exchange Commission.

Indianapolis-based Guidant said Oct. 25 it received a subpoena from the Minneapolis office seeking information on three defibrillators: Ventak Prizm 2, Contak Renewal 1 and Contak Renewal 2. The company's heart-device operations are in Arden Hills.

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