SYNCHROMED II Adverse Event — Injury (MDR 3004209178-2020-07735)
SYNCHROMED II Adverse Event — Injury (MDR 3004209178-2020-07735) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SYNCHROMED II; Generic name: PUMP, INFUSION, IMPLANTED, PROGRAMMABLE; Manufacturer: MDT PUERTO RICO OPERATIONS CO.
| Device | SYNCHROMED II |
|---|---|
| Generic name | PUMP, INFUSION, IMPLANTED, PROGRAMMABLE |
| Manufacturer | MDT PUERTO RICO OPERATIONS CO |
| Report number | 3004209178-2020-07735 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | HEALTH PROFESSIONAL, STUDY |
| Narrative | OTHER RELEVANT DEVICE(S) ARE: PRODUCT ID: 8731SC, SERIAL/LOT #: (B)(4), UBD: 11-SEP-2015, UDI#: (B)(4). THE PUMP WAS RETURNED, AND ANALYSIS FOUND NO ANOMALY. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED. |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →