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Have you or a loved one been injured by an implanted defibrillator from St. Jude Medical due to premature battery depletion?

Find out if you have a           St. Jude Defibrillator case.


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This means getting clients the money and benefits that they deserve. We ensure that our clients are protected at every step of the claims process. We know that coping with an injury or disability is hard enough without added legal stress. Let us take the burden off your shoulders and navigate the legal system on your behalf.

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Almost 400,000 of these cardiac devices were manufactured by St. Jude Medical from January 2010 to May 2015 and feature a faulty design that can short circuit and cause total battery failure in as short a period as 24 hours.

The law office of Becker Law Office can assist in determining if you have one of the St. Jude Medical ICD or CRT-D devices covered by the recall and what your legal options are. We can also help you learn if you are owed compensation due to one of the devices and the complications caused by the need to deal with the situation. We urge you to contact us now and let us do a FREE case review. Because this is a time-sensitive matter, it’s important you fill out the form now so that we can assess your case and contact you if we determine you qualify.

The recall covers Implantable Cardioverter Defibrillators (ICD) and Cardiac Resynchronization Therapy Defibrillators (CRT-D) manufactured and marketed by St. Jude Medical. Here is a list of the devices covered by the FDA recall:

Which St. Jude Medical devices are affected?

The FDA has issued a Class 1 recall, the most serious type of recall, on these devices because of the danger of serious injury or death. Rapid battery failure due to deposits of lithium forming within the battery and triggering a short circuit can cause these pacemaker devices to run out of energy before the patient is aware of the problem or has a chance to have it replaced.

What are possible symptoms of premature battery depletion?

The devices were designed to last approximately 7 years following implantation before needing replacement, but this issue is causing that time period to be reduced unexpectedly if the battery problem surfaces, sometimes with devastating effect. Symptoms may include:

  • Fortify® VR
  • Fortify® ST VR
  • Fortify Assura™ VR
  • Fortify Assura™ ST VR
  • Fortify® DR
  • Fortify® ST DR
  • Fortify Assura™ DR
  • Fortify Assura™ ST DR
  • Unify®
  • Unify Quadra™
  • Unify Assura™
  • Quadra Assura™
  • Quadra Assura MP™
  • Feeling lightheaded
  • Dizziness
  • Loss of consciousness
  • Chest pain
  • Shortness of breath
  • Death

You may be owed damages. Let us begin the process with a FREE case review. Submit the form to the right and we will contact you.