SYNCHROMED II Adverse Event — Injury (MDR 3004209178-2020-07755)
SYNCHROMED II Adverse Event — Injury (MDR 3004209178-2020-07755) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SYNCHROMED II; Generic name: PUMP, INFUSION, IMPLANTED, PROGRAMMABLE; Manufacturer: MEDTRONIC PUERTO RICO OPERATIONS CO..
| Device | SYNCHROMED II |
|---|---|
| Generic name | PUMP, INFUSION, IMPLANTED, PROGRAMMABLE |
| Manufacturer | MEDTRONIC PUERTO RICO OPERATIONS CO. |
| Report number | 3004209178-2020-07755 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | CONSUMER |
| Narrative | CONCOMITANT MEDICAL PRODUCTS: PRODUCT ID: 8780, SERIAL#: (B)(4), IMPLANTED: (B)(6) 2016, PRODUCT TYPE: CATHETER. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED. |
| Source | openFDA MAUDE (device adverse events) |
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