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Saturday, March 15, 2008

The Medtronic Lawsuit

This is a special information for all of us. Just in case you are still not aware, Medtronic Inc. has removed its Sprint Fidelis defibrillation leads from the market after five patient deaths have been linked to the devices. The Medtronic Lawsuit was due to the recall of their products, which was said to be hazardous for one's health. On OCtober 15, 2007 , Medtronic recalled the following products from the market:

• Sprint Fidelis 6930
• Sprint Fidelis 6931
• Sprint Fidelis 6948
• Sprint Fidelis 6949

If you suspect that you maybe affected by these products, consult a doctor or call 1-866-50-RIGHTS (1-866-507-4448) or fill out the online Medtronic Sprint Fidelis case review form today.

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