MEDFUSION 3500 SYRINGE INFUSION PUMP Adverse Event — Malfunction (MDR 2183502-2007-00397)
MEDFUSION 3500 SYRINGE INFUSION PUMP Adverse Event — Malfunction (MDR 2183502-2007-00397) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MEDFUSION 3500 SYRINGE INFUSION PUMP; Generic name: SYRINGE INFUSION PUMP; Manufacturer: SMITHS MEDICAL MD, INC..
| Device | MEDFUSION 3500 SYRINGE INFUSION PUMP |
|---|---|
| Generic name | SYRINGE INFUSION PUMP |
| Manufacturer | SMITHS MEDICAL MD, INC. |
| Report number | 2183502-2007-00397 |
| Event type | Malfunction |
| Product problem | * |
| Date received | 2008-01-24 |
| Report source | User facility |
| Source | openFDA MAUDE (device adverse events) |
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