MEDFUSION Adverse Event — Malfunction (MDR 3012307300-2020-03432)
MEDFUSION Adverse Event — Malfunction (MDR 3012307300-2020-03432) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MEDFUSION; Generic name: PUMP, INFUSION; Manufacturer: SMITHS MEDICAL ASD, INC..
| Device | MEDFUSION |
|---|---|
| Generic name | PUMP, INFUSION |
| Manufacturer | SMITHS MEDICAL ASD, INC. |
| Report number | 3012307300-2020-03432 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | CONSUMER |
| Narrative | ONE MEDFUSION PUMP WAS RECEIVED WITH FLUID CONTAMINATION IN THE PLUNGER HEAD, THE CASE TOP CHIPPED IN CORNERS AND THE BOTTOM CASE GASKET DAMAGED. THE EVENT HISTORY LOG WAS REVIEWED AND THERE WAS A FORCE SENSOR TEST ERROR. THE POWER UP PROCESS WAS CONDUCTED, THE FORCE SENSOR WAS ALSO CHECKED AND TESTED. A FORCE SENSOR ERROR WAS FOUND AT POWER UP. THE FORCE SENSOR VALUE WAS STUCK AND DID NOT CHANGE. |
| Source | openFDA MAUDE (device adverse events) |
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