Contact Us

Guidant Defibrillators
*    Denotes required field.

   * First Name 

   * Last Name 

   * Email 

Phone 

Cell Phone 

Street Address 

Zip Code 

City 

State 

Which Guidant cardiac defibrillator was implanted?








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

Date the device was implanted:

Is the device still implanted?

What medical condition prompted the use of the device?

Please describe any problems or injuries caused by the product:

For verification purposes, please answer the below question:
+
=

No Yes, I agree to the Parker Waichman LLP disclaimers. Click here to review.

Yes, I would like to receive the Parker Waichman LLP monthly newsletter, InjuryAlert.

please do not fill out the field below.


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.


Related articles
Parker Waichman Accolades And Reviews Best Lawyers Find Us On Avvo