MEDFUSION Adverse Event — Malfunction (MDR 3012307300-2020-03425)
MEDFUSION Adverse Event — Malfunction (MDR 3012307300-2020-03425) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MEDFUSION; Generic name: PUMP, INFUSION; Manufacturer: ST PAUL.
| Device | MEDFUSION |
|---|---|
| Generic name | PUMP, INFUSION |
| Manufacturer | ST PAUL |
| Report number | 3012307300-2020-03425 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | USER FACILITY |
| Narrative | INFORMATION WAS RECEIVED INDICATING THAT SMITHS MEDICAL MEDFUSION 4000 PUMP HAS MALFUNCTIONED. IT WAS REPORTED THAT THE PUMP WAS BEING USED INFUSE MEDICATION INTERMITTENTLY WHEN IT STOPPED WHILE INFUSING ANTIBIOTIC (FLAGYL) DESPITE BEING PLUGGED IN. WHEN THE PUMP WAS UNPLUGGED AND IT ALARMED BATTERY LOW. THE REGISTERED NURSE RESPONDED TO THE ALARM AND PLUGGED THE PUMP INTO THE WALL AND THE PUMP ST |
| Source | openFDA MAUDE (device adverse events) |
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