SYNCHROMED II Adverse Event — Injury (MDR 2182207-2008-00806)
SYNCHROMED II Adverse Event — Injury (MDR 2182207-2008-00806) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SYNCHROMED II; Manufacturer: MEDTRONIC NEUROMODULATION; Report number: 2182207-2008-00806.
| Device | SYNCHROMED II |
|---|---|
| Manufacturer | MEDTRONIC NEUROMODULATION |
| Report number | 2182207-2008-00806 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-19 |
| Report source | Consumer |
| Narrative | THE PATIENT REPORTED THAT HER DEVICES WERE REMOVED DUE TO AN INFECTION. NO SYMPTOMS WERE REPORTED. THE TYPE OF MEDICATION, CONCENTRATION, AND DAILY DOSE BEING ADMINISTERED VIA THE PUMP WERE NOT REPORTED; DEVICE REGISTRATION SYSTEM INDICATES FENTANYL. ADDITIONAL INFORMATION HAS BEEN REQUESTED, A FOLLOW-UP REPORT WILL BE SENT IF ADDITIONAL INFORMATION BECOMES AVAILABLE. |
| Source | openFDA MAUDE (device adverse events) |
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