DEEP BRAIN STIMULATION LEAD Adverse Event — Injury (MDR 6000153-2008-00730)
DEEP BRAIN STIMULATION LEAD Adverse Event — Injury (MDR 6000153-2008-00730) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: DEEP BRAIN STIMULATION LEAD; Manufacturer: MEDTRONIC PUERTO RICO OPERATIONS CO.; Report number: 6000153-2008-00730.
| Device | DEEP BRAIN STIMULATION LEAD |
|---|---|
| Manufacturer | MEDTRONIC PUERTO RICO OPERATIONS CO. |
| Report number | 6000153-2008-00730 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-15 |
| Report source | Consumer, Health Professional |
| Narrative | THE PATIENT REPORTED INTERMITTENT TINGLING FROM THEIR LEFT HAND TO LEFT SHOULDER FOR THE LAST WEEK. THE PATIENT ALSO REPORTED A LOSS OF EFFICACY OCCURS. THE PATIENT NOTED A BLINKING LIGHT ON THEIR PROGRAMMER. FOLLOW UP WITH THE HCP INDICATED THE TINGLING WAS MOST NOTED IN THE EVENING. THE HCP FELT IT MAY BE RELATED TO INCREASED BASELINE PARKINSON'S SYMPTOMS AND THE BLINKING LIGHT WAS INDICATING TH |
| Source | openFDA MAUDE (device adverse events) |
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