PRECISION Adverse Event — Injury (MDR 3006630150-2020-01899)
PRECISION Adverse Event — Injury (MDR 3006630150-2020-01899) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PRECISION; Generic name: STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF; Manufacturer: BOSTON SCIENTIFIC NEUROMODULATION.
| Device | PRECISION |
|---|---|
| Generic name | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF |
| Manufacturer | BOSTON SCIENTIFIC NEUROMODULATION |
| Report number | 3006630150-2020-01899 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, HEALTH |
| Narrative | EXPLANT DATE: 2012. MODEL NUMBER/ CATALOG NUMBER: SC-2218-50, SERIAL NUMBER: (B)(4), BATCH/ LOT NUMBER: 14140205 / 14140205, MODEL/ CATALOG DESCRIPTION: LINEAR ST LEAD KIT 50 CM. THE EXPLANTED DEVICES WERE NOT RETURNED TO BSN. |
| Source | openFDA MAUDE (device adverse events) |
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