SYNCHROMED II Adverse Event — Injury (MDR 2182207-2008-00797)
SYNCHROMED II Adverse Event — Injury (MDR 2182207-2008-00797) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SYNCHROMED II; Manufacturer: MEDTRONIC NEUROMODULATION; Report number: 2182207-2008-00797.
| Device | SYNCHROMED II |
|---|---|
| Manufacturer | MEDTRONIC NEUROMODULATION |
| Report number | 2182207-2008-00797 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-19 |
| Report source | Consumer |
| Narrative | THE PATIENT'S WIFE REPORTED THAT THE PATIENT HAD A HIGH FEVER, MUSCLE CONTRACTION, A DROP IN BLOOD PRESSURE AND WAS ADMITTED TO THE INTENSIVE CARE UNIT OF THE HOSPITAL. THE PATIENT WAS RECEIVING BACLOFEN VIA THE PUMP. THE PATIENT WAS ALSO RECEIVING ORAL BACLOFEN AND VALIUM. NO PUMP ALARMS HAD BEEN HEARD AND NO DEVICE TROUBLESHOOTING HAD BEEN DONE. THE PATIENT'S WIFE WAS ENCOURAGED TO CONTACT THE P |
| Source | openFDA MAUDE (device adverse events) |
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