| Nombre | Clasificación | Fabricante | Nivel de riesgo | País | Fuente |
|---|---|---|---|---|---|
| SynchroMed II Pump | Medtronic | Sweden | SMPA | ||
| SynchroMed Implantable Infusion Pump | Medtronic Inc. | Turkey | TDMDAT | ||
| Device Recall Synchromed II | General Hospital and Personal Use Devices | Medtronic Inc, Neurological & Spinal Division | 2 | United States | USFDA |