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Federal Preemption Update: March 2009 Supreme Court Decision

Free Case Evaluation

MEDTRONIC SPRINT FIDELIS LEAD WIRE CASE EVALUATION

Our law firm represents people in personal injury and wrongful death cases that involve adverse medical events caused by the Sprint Fidelis electrical lead wires used in some heart devices such as implantable cardioverter defibrillators (ICD) and cardiac resynchronization therapy-defibrillators (CRT-D) breaking or fracturing.

These Medtronic Sprint Fidelis leads can break or fracture and cause a massive unnecessary shock to the patient's heart, resulting in personal injury, or cause the defibrillator battery to go dead, which causes the implantable heart device to fail to delivery a necessary life-saving shock, and resulting in death.

Please be assured that the information you provide to our law firm when completing this legal case evaluation form will be treated by us as strictly confidential.

Personal Information

*Required Fields

*Your Name:

*E-mail:

Street Address:

City:

State:

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*Phone Number:

Best time to call: DayNight

Case Facts

1. Do you, a family member, or some other person you know have a defibrillator that was implanted at some time between September 1, 2004 and the present?
YesNoYes, but I am not sure of the exact date

2. Have you or a person you know suffered an adverse medical event caused by a defibrillator that might have been using the Sprint Fidelis lead wire? YesNo

3. Would the case you are describing be a personal injury case or a wrongful death case:
Wrongful DeathPersonal Injury

4. Is this for you or someone else, and if it is for someone else, what is his or her relationship to you? MeSomeone Else
Relationship:

5. If there was a death possibly caused by the defective defibrillator lead wire, on what date did it occur:

6. What is the date of birth of the person who suffered the lead wire defibrillator malfunction, if known:

7. Has a lawsuit been filed concerning the possible Medtronic Sprint Fidelis case: YesNo

Is there any additional information you would like to include?

Please enter any additional information about this claim, as well as any comments or questions you may have, in the following space:

  • US FDA advises that you should not stop taking any prescription medication before talking to your doctor.
  • Reports of serious drug side effects should be made to the US FDA MedWatch program.
  • The prescription drug names are registered trademarks of the respective drug companies.
  • DrugInjuryLaw.com is not affiliated with any of the drug companies, nor US FDA.
Law Offices of Thomas J. Lamb, P.A.
Lumina Station Suite 225
1908 Eastwood Road
Wilmington, NC 28403
Tel: (910) 256-2971   Fax: (910) 256-2972
Toll Free: (800) 426-9535
email: ThomasJLamb@DrugInjuryLaw.com
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