INTRATHECAL CATHETER Adverse Event — Malfunction (MDR 6000030-2008-00760)
INTRATHECAL CATHETER Adverse Event — Malfunction (MDR 6000030-2008-00760) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: INTRATHECAL CATHETER; Manufacturer: RICE CREEK MANUFACTURING; Report number: 6000030-2008-00760.
| Device | INTRATHECAL CATHETER |
|---|---|
| Manufacturer | RICE CREEK MANUFACTURING |
| Report number | 6000030-2008-00760 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-15 |
| Report source | Health Professional |
| Narrative | THE HCP REPORTED THE PATIENT WAS NOT GETTING THE NEEDED SPASTICITY RELIEF. THE PUMP WAS EXPLANTED AND REPLACED AFTER AN IMPLANT DURATION OF 6 MONTHS. ADDITIONAL INFORMATION FROM THE HCP REPORTED THE PATIENT WAS EXPERIENCING INCREASED SPASTICITY AND PAIN. THE HCP REPORTED HE "WENT THROUGH EVERYTHING DIAGNOSTICALLY INCLUDING MYELOGRAM THROUGH PUMP ACCESS PORT. AT SURGERY, CATHETER (DISTAL) WAS WRAPP |
| Source | openFDA MAUDE (device adverse events) |
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