SPECIFY Adverse Event — Injury (MDR 2182207-2008-00687)
SPECIFY Adverse Event — Injury (MDR 2182207-2008-00687) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SPECIFY; Manufacturer: MEDTRONIC INC. NEUROLOGICAL DIVISION; Report number: 2182207-2008-00687.
| Device | SPECIFY |
|---|---|
| Manufacturer | MEDTRONIC INC. NEUROLOGICAL DIVISION |
| Report number | 2182207-2008-00687 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-15 |
| Report source | Consumer, Health Professional |
| Narrative | THE PT'S HUSBAND HAD PREVIOUSLY REPORTED, THAT WHEN THE NEUROSTIMULATOR WAS TURNED ON, IT CAUSED HIS WIFE (THE PATIENT) TO HAVE ACUTE PAIN AND DIFFICULTY WALKING. THE PAIN WAS LOCATED AT THE PARESTHESIA AREA. HE INCLUDED THAT IN 2007, "IT WAS SO PAINFUL THAT SHE FELL DOWN AND HIT HER HEAD". SEE MANUFACTURER'S REPORT # 6000032200800049. THE HCP REPORTED, THAT INITIALLY THE PT'S NEUROSTIMULATOR WAS |
| Source | openFDA MAUDE (device adverse events) |
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