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ALERTS!

Medtronic Leads
Gadolinium
Avandia
Kugel Mesh Patch
Ortho Evra
 

 

 


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The Hollis Law Firm

5100 West 95th Street

Prairie Village,  KS  66207

1-800-701-3672

 

 

 
 

Defective Medtronic Leads Result in Nationwide Deaths and Injuries
 

Medtronic has taken  their Sprint FidelisŪ defibrillator leads off the market.  These leads have fractured, which can result in the defibrillators delivering unnecessary shocks.  The lead fractures have been linked to the deaths of five individuals.  Medtronic manufactured more than 235,000 of these leads in the United States.  Medtronic has asked that all of the leads that have not been implanted be returned to Medtronic.  They have also advised doctors to contact their patients who have these leads implanted in them.  The recalled devices are:

  • Sprint FidelisŪ 6930

  • Sprint FidelisŪ 6948

  • Sprint FidelisŪ 6949  

  • Sprint FidelisŪ 6931

 
FAQ's
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FDA Warnings:

Do You Have a Medtronic Inc. Sprint FidelisŪ Defibrillator Lead?  

Have you had an MRI with Contrast Dye? 

Have you suffered a heart attack or congestive heart failure while on Avandia? 

Have you had a Kugel Mesh hernia patch that broke?

 

 

 
1-800-701-3672

The Hollis Law Firm       5100 West 95th Street       Prairie Village,  Kansas        66207

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