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Medtronic Recall - Medtronic Pacemaker Recall WarningsADDITIONAL MEDTRONIC RECALL:

Another Medtronic recall involved the Micro Jewel® II Model 7223Cx and the GEM® DR Model 7271. This Medtronic recall occurred on April 16th 2004, was made because these units could have defective high voltage capacitors. As a result of this defect, the capacitors may take longer than normal to charge. This delay in charging could cause a resultant delay in the delivery of the electrical pulse therapy.

All of these recalls are considered Class I recalls by the Food and Drug Administration (FDA). Class I recalls are the most serious type because they involve a reasonable probability that continued use of the product will result in either serious injury or death.

If you or someone you know has or had a Medtronic device implanted, and you would like to find out more, please contact our Medtronic Recall Lawyers and an experienced attorney will respond to you shortly.
 


 
 MEDTRONIC PACEMAKER RECALL

Medtronic Recall - Medtronic Pacemaker ICD


Medtronic Recall - Medtronic Recall LawyersDoes the Medtronic Pacemaker Recall affect you?  Call our Medtronic Recall Hotline now to find out.

1-800-606-0036 24 hour Medtronic Recall Hotline

 
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