MEDFUSION Adverse Event — Malfunction (MDR 3012307300-2020-03386)
MEDFUSION Adverse Event — Malfunction (MDR 3012307300-2020-03386) 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 | 3012307300-2020-03386 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | CONSUMER |
| Narrative | ONE MEDFUSION PUMP WAS RECEIVED WITH THE FRONT CORNERS OF THE TOP AND BOTTOM CASES DAMAGED. THE EVENT HISTORY WAS REVIEWED AND THERE WAS A MOTOR NOT RUNNING ERROR IN THE HISTORY. A FLOW TEST WAS CONDUCTED AND THE REPORTED ISSUE WAS CONFIRMED. THE MAIN BOARD WAS NOT SEATED INTO THE DROVE OF THE EXTRUSION. THE ISSUE WAS A RESULT OF THE CUSTOMER'S IMPACT TO THE DEVICE. THE MAIN BOARD WAS INSTALLED ON |
| Source | openFDA MAUDE (device adverse events) |
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