UNK Adverse Event — Injury (MDR 2182207-2008-00782)
UNK Adverse Event — Injury (MDR 2182207-2008-00782) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNK; Manufacturer: MEDTRONIC NEUROMODULATION; Report number: 2182207-2008-00782.
| Device | UNK |
|---|---|
| Manufacturer | MEDTRONIC NEUROMODULATION |
| Report number | 2182207-2008-00782 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-19 |
| Report source | Study, Literature, Health Professional |
| Narrative | JOURNAL REFERENCE: PHILLIPS ET AL. "IMAGING APPEARANCE OF INTRATHECAL CATHETER TIP GRANULOMAS: REPORT OF THREE CASES AND REVIEW OF THE LITERATURE." AM J ROENTGENOL 2007; 189(6): 1524. THREE PATIENTS WHO RECEIVED A SPINAL CATHETER FOR INTRATHECAL ADMINISTRATION OF OPIOIDS UNDERWENT SURGERY FOR REMOVAL OF AN INFLAMMATORY MASS AT THE INTRATHECAL CATHETER TIP. REPORTABLE EVENT: A WOMAN WITH FAILED BAC |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →