CADD Adverse Event — Malfunction (MDR 3012307300-2020-03398)
CADD Adverse Event — Malfunction (MDR 3012307300-2020-03398) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CADD; Generic name: PUMP, INFUSION; Manufacturer: ST PAUL.
| Device | CADD |
|---|---|
| Generic name | PUMP, INFUSION |
| Manufacturer | ST PAUL |
| Report number | 3012307300-2020-03398 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | USER FACILITY |
| Narrative | INFORMATION WAS RECEIVED INDICATING THAT DURING TESTING, A SMITHS MEDICAL CADD SOLIS VIP PUMP FAILED THE VOLUME TEST. NO PATIENT WAS INVOLVED IN THIS EVENT. NO ADVERSE EFFECTS WERE REPORTED. |
| Source | openFDA MAUDE (device adverse events) |
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