PRECISION Adverse Event — Injury (MDR 2029203-2008-00090)
PRECISION Adverse Event — Injury (MDR 2029203-2008-00090) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PRECISION; Generic name: SPINAL CORD STIMULATOR LEAD; Manufacturer: BOSTON SCIENTIFIC NEUROMODULATION CORP..
| Device | PRECISION |
|---|---|
| Generic name | SPINAL CORD STIMULATOR LEAD |
| Manufacturer | BOSTON SCIENTIFIC NEUROMODULATION CORP. |
| Report number | 2029203-2008-00090 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-21 |
| Report source | Health Professional |
| Narrative | DURING A LEAD PLACEMENT PROCEDURE, IT WAS CONFIRMED THAT THE PT HAD A DURA PUNCTURE. THE PT WAS ADMINISTERED A BLOOD PATCH AND IS REPORTEDLY DOING WELL. |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →