CADD SOLIS VIP PUMP Adverse Event — Malfunction (MDR 3012307300-2020-03390)
CADD SOLIS VIP PUMP Adverse Event — Malfunction (MDR 3012307300-2020-03390) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CADD SOLIS VIP PUMP; Generic name: PUMP, INFUSION; Manufacturer: ST PAUL.
| Device | CADD SOLIS VIP PUMP |
|---|---|
| Generic name | PUMP, INFUSION |
| Manufacturer | ST PAUL |
| Report number | 3012307300-2020-03390 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Narrative | INFORMATION WAS RECEIVED INDICATING THAT A SMITHS MEDICAL DEVICE WAS EXHIBITING A CONSTANT AIR-IN-LINE ALARM WITH PRIMED TUBING. THERE WAS NO REPORTED ADVERSE EVENT. |
| Source | openFDA MAUDE (device adverse events) |
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