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Heart Defibrillators Recalled

Implantable Heart Defibrillators have been RECALLED by Guidant Corporation because of potential electrical malfunctions. These recalls include:

  • Contak Renewal Model H135 CRT-D
    manufactured on or before August 26, 2004
  • Contak Renewal Model H155 CRT-D
    manufactured on or before August 26, 2004
  • Ventak Prizm 2 DR Model 1861
    manufactured on or before April 16, 2002
  • Ventak Prizm AVT (all series numbers)
  • Vitality AVT (all series numbers)
  • Renewal 3 AVT (all series numbers)
  • Renewal 4 AVT (all series numbers)

If you or members of your family have one of the defibrillators listed above, you may have a claim for damages. For information concerning your legal rights, complete the information below and press the SUBMIT button.

DAVID GRONER
ACCIDENT & INJURY ATTORNEYS
POST OFFICE BOX 9207
NEW IBERIA, LA 70560
(337) 364-3629 OR (877) 732-4537
FAX: (337) 367-2438
www.davidgroner.com

NAME:

ADDRESS:

CITY STATE ZIP:

DOB:

TEL. NUMBER:

CHECK MODEL BELOW:

CONTAK RENEWAL MODEL H135
CONTAK RENEWAL MODEL H155
VENTAK PRIZM 2DR MODEL 1861
VENTAK PRIZM AVT (all series numbers)
VITALITY AVT (all series numbers)
RENEWAL 3 AVT (all series numbers)
RENEWAL 4 AVT (all series numbers)

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Louisiana Accident and Injury Attorneys

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