DEEP BRAIN STIMULATOR LEAD Adverse Event — Death (MDR 2182207-2008-00770)
DEEP BRAIN STIMULATOR LEAD Adverse Event — Death (MDR 2182207-2008-00770) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: DEEP BRAIN STIMULATOR LEAD; Manufacturer: MEDTRONIC NEUROMODULATION; Report number: 2182207-2008-00770.
| Device | DEEP BRAIN STIMULATOR LEAD |
|---|---|
| Manufacturer | MEDTRONIC NEUROMODULATION |
| Report number | 2182207-2008-00770 |
| Event type | Death |
| Product problem | N |
| Date received | 2008-02-19 |
| Report source | Foreign, Study, Literature, Health Professional |
| Narrative | JOURNAL REFERENCE; PATRICK ET AL. "DEEP BRAIN STIMULATION OF THE INTERNAL PALLIDUM IN MULTIPLE SYS ATROPHY --CASE REPORT" PARKINSONISM & RELATED DISORDERS/2006/12/181-183. THE ARTICLE IS A CASE STUDY OF ONE MALE PT WITH MULTIPLE SYS ATROPHY WHO WAS TREATED WITH BILATERAL DBS OF THE INTERNAL PALLIDUM. REPORTABLE EVENT: PT DIED SUDDENLY 7 MOS POST-OPERATIVELY, PROBABLY DUE TO PULMONARY EMBOLISM. AUT |
| Source | openFDA MAUDE (device adverse events) |
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