Pacemaker Defects
Ennis & Ennis, P.A. is also currently handling lawsuits for the following drugs: Accutane, Actiq, Adderall, Avandia, Bextra, Celebre, Fosamax, Ketek, Ortho Evra Birth Control Patch, Paxil, Plavix, Serevent, Seroquel, Tequin, Trasylol, Viagra, Vioxx, Zelnorm & Zyprexa.
 
Medtronic Lawsuit
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Ennis & Ennis, P.A. is representing individuals that have been harmed as a result of Medtronic defibrillator or pacemaker defects. If you or a loved one have been injured you may be entitled to compensation. For more information about your legal rights or for more information regarding the Medtronic recall click here to contact one of our Medtronic Attorneys about a Medtronic lawsuit today.

 

Cardiac implants caused loss of enjoyment of life

-Southeast Texas Record


01/31/2008 - To treat life-threatening heart conditions, Texas residents Lawrence Booth and Larry Easter were given implantable cardiac defibrillators (ICD), to detect and correct both fast and slow heart rates. But the men believe the ICD's have caused them pain and suffering and have filed a lawsuit against the manufacturer.

Booth and Easter filed a product liability suit against Medtronic, Medtronic Puerto Rico, and Medtronic Puerto Rico Operations Company on Jan. 28 in the Texarkana Division of the Eastern District of Texas.

According to the plaintiffs' original complaint, both men are implanted with an ICD that contains a Sprint Fidelis 6948 lead wire system, which is subject to a voluntary recall by manufacturer Medtronic.

On Oct. 15, 2007, Medtronic voluntarily suspended distribution of the Sprint Fidelis Leads (models: 6930, 6931, 6948, and 6949) because of a potential for lead factures.

The plaintiffs claim the ICD's are causing them to suffer "severe physical and emotional injuries, pain and suffering, medical expenses, and loss of enjoyment of life."

The lawsuit is demanding claims of relief for products liability, breach of warranty, and negligence.

Booth and Easter are seeking punitive and exemplary damages for medical expenses, pain and suffering, lost wages, physical impairment, mental anguish, pre and post-judgment interest, and costs of suit.

According to the Medtronic news release, worldwide approximately 268,000 Sprint Fidelis leads have been implanted. Doctors and medical experts advise against patients seeking unnecessary replacement as the risk of removal far exceeds the risk of a lead failure.

U.S. District Judge David Folsom is assigned to the litigation.

Ennis & Ennis, P.A. is representing individuals that have been harmed defective medical devices such as the Medtronic defibrillator and pacemaker. If you or a loved one have suffered as a result of a defective Medtronic pacemaker or defibrillator or if you need more information about the Medtronic recall or class action lawsuit click here for a free, confidential case evaluation.

 

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