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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
Recall Date to: 09/01/2015 PMA Number: P920015
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Product Description
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FDA Recall
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Medtronic Sprint Fidelis 6930 Steroid eluting, tripolar, ventricular lead with tined tip and right v... 1 10/25/2007 Medtronic Inc. Cardiac Rhythm Managment
Medtronic Sprint Fidelis 6931 Steroid eluting, tripolar, screw-in, ventricular lead with right ventr... 1 10/25/2007 Medtronic Inc. Cardiac Rhythm Managment
Medtronic Sprint Fidelis 6948 Steroid eluting, quadripolar, ventricular lead with tined tip and righ... 1 10/25/2007 Medtronic Inc. Cardiac Rhythm Managment
Medtronic Sprint Fidelis 6949 Steroid eluting, quadripolar, screw-in, ventricular lead with right ve... 1 10/25/2007 Medtronic Inc. Cardiac Rhythm Managment
Medtronic Sprint Quattro Secure S, model 6935. Steroid eluting, tripolar, screw-in, ventricular lea... 2 11/26/2010 Medtronic Inc. Cardiac Rhythm Disease Managment
Medtronic Sprint Quattro Secure, model 6947. Steroid eluting, quadripolar, screw-in, ventricular le... 2 11/26/2010 Medtronic Inc. Cardiac Rhythm Disease Managment
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