Medical Device Recalls
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61 to 66 of 66 Results
Recall Date to: 08/04/2015 PMA Number: P860004 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Medtronic SynchroMed II Programmable Pump, model 8637-40. The contents of the inner package have be... | 1 | 03/22/2008 | Medtronic Neuromodulation |
Medtronic SynchroMed EL Programmable Pump, Model 8626-10. Medtronic, Inc., 710 Medtronic Parkway, M... | 1 | 02/02/2008 | Medtronic Neuromodulation |
Medtronic SynchroMed EL Programmable Pumps, Models 8627-10, 8627-18, 8627L-10, 8627L-18. The implan... | 1 | 10/20/2006 | Medtronic Neuromodulation |
Medtronic Intrathecal Catheter, Model 8731, (part of infusion systems using Medtronic implantable pu... | 1 | 09/09/2006 | Medtronic Neurological |
Medtronic Intrathecal Catheter Distal Revision Kit, Model 8598, (provides replacement parts for the ... | 1 | 09/09/2006 | Medtronic Neurological |
8870 software application card versions AAA 02, BBB 04, BBC 02, and BBD 01, which is used in conjunc... | 1 | 09/23/2004 | Medtronic Inc, Neurological & Spinal Division |
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