MEDFUSION Adverse Event — Malfunction (MDR 3012307300-2020-03430)
MEDFUSION Adverse Event — Malfunction (MDR 3012307300-2020-03430) 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 | 3012307300-2020-03430 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | CONSUMER |
| Narrative | ONE MEDFUSION PUMP WAS RECEIVED WITH BOTH FRONT CORNERS OF THE TOP CASE CRACKED, A CRACKED RIGHT PLUNGER CASE AND MISSING A PORTION OF THE BOTTOM CASE SEAL. THE EVENT HISTORY LOG WAS REVIEWED AND THERE WAS A "PUMP MOTOR DRIVE OFF POST" MESSAGE. THE POWER UP PROCESS WAS CONDUCTED AND THE PUMP MOTOR DRIVE OFF POST WAS FOUND AT POWER UP. THE BATTERY WAS FOUND NOT CHARGING DUE TO CONTAMINATION (DRY) F |
| Source | openFDA MAUDE (device adverse events) |
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