N'VISION Adverse Event — Injury (MDR 2182207-2008-00697)
N'VISION Adverse Event — Injury (MDR 2182207-2008-00697) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: N'VISION; Manufacturer: MEDTRONIC NEUROMODULATION; Report number: 2182207-2008-00697.
| Device | N'VISION |
|---|---|
| Manufacturer | MEDTRONIC NEUROMODULATION |
| Report number | 2182207-2008-00697 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-15 |
| Report source | Health Professional, Company representation |
| Narrative | THE HCP REPORTED, THAT THE PATIENT HAD NORMAL SALINE IN HER PUMP WHICH WAS CHANGED TO DILAUDID 1 MG/DAY AND BUPIVACAINE. A PROGRAMMING ERROR OCCURRED; ONLY THE CATHETER WAS PRIMED. IN 2008, THE PATIENT RETURNED TO THE CLINIC WITH INCREASED PAIN. THE INFUSION RATE WAS INCREASED TO 2 MG/DAY. THE PREVIOUS PROGRAMMING ERROR WAS NOT NOTICED. THE EMERGENCY ROOM DOCTOR CALLED THE PATIENT'S HCP STATING, T |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →