MEDFUSION Adverse Event — Malfunction (MDR 3012307300-2020-03379)
MEDFUSION Adverse Event — Malfunction (MDR 3012307300-2020-03379) 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 | 3012307300-2020-03379 |
| Event type | Malfunction |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | CONSUMER |
| Narrative | ONE MEDFUSION PUMP WAS RECEIVED WITH THE BOTTOM CASE CRACKED BY THE "L" BRACKET POLE CLAMP. THE PLUNGER HEAD WAS CRACKED BY SCREWS. THERE WAS NO DAMAGE ON TOP CASE AND NO VISIBLE CONTAMINATION. THE EVENT HISTORY LOG WAS REVIEWED AND THERE WAS A PRIMARY AUDIBLE BACKGROUND TEST IN THE HISTORY. THE PUMP WAS POWERED ON, INFUSION AND OCCLUSION TESTS WERE ALSO PERFORMED. THE REPORTED ISSUE WAS UNABLE TO |
| Source | openFDA MAUDE (device adverse events) |
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