CADD SOLIS VIP PUMP Adverse Event — Malfunction (MDR 3012307300-2020-03467)
CADD SOLIS VIP PUMP Adverse Event — Malfunction (MDR 3012307300-2020-03467) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CADD SOLIS VIP PUMP; Generic name: PUMP, INFUSION; Manufacturer: SMITHS MEDICAL ASD, INC..
| Device | CADD SOLIS VIP PUMP |
|---|---|
| Generic name | PUMP, INFUSION |
| Manufacturer | SMITHS MEDICAL ASD, INC. |
| Report number | 3012307300-2020-03467 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | CONSUMER |
| Narrative | INFORMATION WAS RECEIVED INDICATING THAT DURING TESTING OF A SMITHS MEDICAL CADD-SOLIS VIP AMBULATORY INFUSION PUMP FAILED FLOW RATE TESTING TWICE BY -7.2 PERCENT AND -6.8 PERCENT. THERE WAS NO PATIENT INVOLVEMENT WITH NO REPORTED ADVERSE EFFECTS. |
| Source | openFDA MAUDE (device adverse events) |
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