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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 8 of 8 Results
Recall Date to: 11/27/2015 PMA Number: P860004/S081
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Medtronic Sutureless Pump Connector Revision Kit, model 8578. Contents: catheter interface with at... 1 06/24/2013 Medtronic Neuromodulation
Medtronic Intrathecal Catheter Pump Segment Revision Kit, model 8596SC. Contents: 60-cm pump segme... 1 06/24/2013 Medtronic Neuromodulation
Medtronic INDURA 1P Intrathecal Catheter, model 8709SC. Contents: 81.4-cm catheter with length mar... 1 06/24/2013 Medtronic Neuromodulation
Medtronic Intrathecal Catheter, model 8731SC. Contents: 38.1-cm spinal segment with length marking... 1 06/24/2013 Medtronic Neuromodulation
Medtronic Indura 1P Intrathecal Catheter, model 8709SC, Method of Sterilization: Ethylene Oxide. M... 1 09/10/2009 Medtronic Neuromodulation
Medtronic Intrathecal Catheter, model 8731SC, Method of Sterilization: Ethylene Oxide. Medtronic, ... 1 09/10/2009 Medtronic Neuromodulation
Medtronic Intrathecal Catheter Pump Segment Revision Kit, model 8596SC, Method of Sterilization: Et... 1 09/10/2009 Medtronic Neuromodulation
Medtronic Sutureless Pump Connector Revision Kit, model 8578, Method of Sterilization: Ethylene Oxi... 1 09/10/2009 Medtronic Neuromodulation
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