NEUROBLATE SYSTEM Adverse Event — Injury (MDR 3009970070-2020-00037)
NEUROBLATE SYSTEM Adverse Event — Injury (MDR 3009970070-2020-00037) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: NEUROBLATE SYSTEM; Generic name: NEUROBLATE® SYSTEM; Manufacturer: MONTERIS MEDICAL.
| Device | NEUROBLATE SYSTEM |
|---|---|
| Generic name | NEUROBLATE® SYSTEM |
| Manufacturer | MONTERIS MEDICAL |
| Report number | 3009970070-2020-00037 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE |
| Narrative | IT WAS REPORTED THAT FOLLOWING THE ABLATION PROCEDURE, THE PATIENT EXPERIENCED WORSENED SENSORY LOSS IN THE LEFT FACE AND ARM. THERE WERE NO FURTHER PATIENT COMPLICATIONS REPORTED IN RELATION TO THIS EVENT. |
| Source | openFDA MAUDE (device adverse events) |
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