SYNCHROMED II Adverse Event — Injury (MDR 3004209178-2008-00708)
SYNCHROMED II Adverse Event — Injury (MDR 3004209178-2008-00708) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SYNCHROMED II; Manufacturer: MEDTRONIC PUERTO RICO OPERATIONS CO.; Report number: 3004209178-2008-00708.
| Device | SYNCHROMED II |
|---|---|
| Manufacturer | MEDTRONIC PUERTO RICO OPERATIONS CO. |
| Report number | 3004209178-2008-00708 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-15 |
| Report source | Consumer |
| Narrative | THE PATIENT REPORTED THAT THE SYSTEM HAD BEEN "REMOVED ABOUT TWO WEEKS POST SURGERY DUE TO AN INFECTION." ADDITIONAL INFORMATION HAS BEEN REQUESTED FROM THE PHYSICIAN. |
| Source | openFDA MAUDE (device adverse events) |
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