Defibrillator Recall

Did you know that on October 15, 2007, Medtronic Inc, the company behind Sprint Fidelis made a product recall on the market. Most defibrillator and pacemaker patients have an identification card that lists the model and serial numbers of their devices and leads. If you look at your identification card and see the numbers 6930, 6931, 6948 or 6949, it is likely that you have a recalled lead. The following products are said to be hazardous to ones health, and the public was warned of these. The items under Defibrillator Recall are the following

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

If you suspect to be a victim of this product, or you were simply exposed to these materials, consult your doctor immediately or call 1-866-9-MEDTRONIC for a free consultation. It is always best to be on the safe side and stay healthy after all.