MEDFUSION Adverse Event — Malfunction (MDR 3012307300-2020-03440)
MEDFUSION Adverse Event — Malfunction (MDR 3012307300-2020-03440) 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 | 3012307300-2020-03440 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | CONSUMER |
| Narrative | INFORMATION WAS RECEIVED INDICATING THAT A SMITHS MEDICAL MEDFUSION PUMP HAD A SYRINGE SENSOR ERROR. THE ISSUE WAS DISCOVERED DURING A SERVICE CHECK AND THERE WAS NO PATIENT INVOLVEMENT. |
| Source | openFDA MAUDE (device adverse events) |
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