SYNCHROMED II Adverse Event — Injury (MDR 2182207-2008-00723)
SYNCHROMED II Adverse Event — Injury (MDR 2182207-2008-00723) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SYNCHROMED II; Manufacturer: MEDTRONIC NEUROMODULATION; Report number: 2182207-2008-00723.
| Device | SYNCHROMED II |
|---|---|
| Manufacturer | MEDTRONIC NEUROMODULATION |
| Report number | 2182207-2008-00723 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-15 |
| Report source | Health Professional |
| Narrative | IT WAS REPORTED THAT THE PT HAS BEEN UNCONSCIOUS FOR A WEEK . THE HCP DID NOT BELIEVE INITIALLY THAT THE PT'S CONDITION WAS DUE TO THE DRUG, BUT NOW PLANNED TO LOWER THE DOSE OF DRUG BEING DELIVERED BY THE PUMP. THE DRUG USED IN THE PUMP WAS MORPHINE. A FOLLOW UP REPORT WILL BE SENT IF ADD'L INFO BECOMES AVAILABLE TO US. |
| Source | openFDA MAUDE (device adverse events) |
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