MEDFUSION Adverse Event — Malfunction (MDR 3012307300-2020-03455)
MEDFUSION Adverse Event — Malfunction (MDR 3012307300-2020-03455) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MEDFUSION; Manufacturer: ST PAUL; Report number: 3012307300-2020-03455.
| Device | MEDFUSION |
|---|---|
| Manufacturer | ST PAUL |
| Report number | 3012307300-2020-03455 |
| 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 DEVICE'S BATTERY DEPLETED. IT WAS ALSO INDICATED THAT THE PUMP'S BASE WAS NOT RESPONDING. THERE WERE NO ADVERSE EVENTS REPORTED. |
| Source | openFDA MAUDE (device adverse events) |
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