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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
Recall Date to: 04/25/2015 PMA Number: P970004
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FDA Recall
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Medtronic InterStim II INS Model 3058 with N'Vision InterStim-B Software supplied on the Model 8870 ... 2 10/11/2007 Medtronic Neuromodulation
Medtronic InterStim INS (Model 3023) with N'Vision Inter Stim-B software supplied on the Model 8870 ... 2 10/12/2007 Medtronic Neuromodulation
Medtronic iCon Patient Programmer, model 3037. The Patient programmer is a hand held, battery opera... 3 09/20/2008 Medtronic Neuromodulation
The Medtronic, Quadripolar ITREL 3 IPG, Model 7425, is a multiprogrammable device designed for use i... 2 06/26/2015 Medtronic Neuromodulation
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