MEDFUSION 4000 SYRINGE PUMP Adverse Event — Malfunction (MDR 3012307300-2020-03406)
MEDFUSION 4000 SYRINGE PUMP Adverse Event — Malfunction (MDR 3012307300-2020-03406) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MEDFUSION 4000 SYRINGE PUMP; Generic name: PUMP, INFUSION; Report number: 3012307300-2020-03406.
| Device | MEDFUSION 4000 SYRINGE PUMP |
|---|---|
| Generic name | PUMP, INFUSION |
| Report number | 3012307300-2020-03406 |
| 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 GAVE A NEAR EMPTY ALERT. THE REGISTERED NURSE WENT TO PUT FLUSH ON MEDICATION AND GOT A BIOMED ERROR. THERE WERE NO ADVERSE EVENTS REPORTED. |
| Source | openFDA MAUDE (device adverse events) |
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