CADD LEGACY PLUS PUMP Adverse Event — Malfunction (MDR 3012307300-2020-03448)
CADD LEGACY PLUS PUMP Adverse Event — Malfunction (MDR 3012307300-2020-03448) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CADD LEGACY PLUS PUMP; Generic name: PUMP, INFUSION; Manufacturer: SMITHS MEDICAL ASD, INC..
| Device | CADD LEGACY PLUS PUMP |
|---|---|
| Generic name | PUMP, INFUSION |
| Manufacturer | SMITHS MEDICAL ASD, INC. |
| Report number | 3012307300-2020-03448 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | DISTRIBUTOR |
| Narrative | DEVICE EVALUATION: ONE CADD SOLIS VIP PUMP WAS RETURNED FOR ANALYSIS. VISUAL INSPECTION WAS PERFORMED. ACCORDING TO THE INVESTIGATION, EVENT HISTORY LOG WAS NOT AVAILABLE. THE CUSTOMER'S REPORTED PROBLEM WAS CONFIRMED. THE PUMP WAS FOUND TO BE DISPLAYING "1260" ERROR CODE ALARM MESSAGE ON POWER UP DURING THE INVESTIGATION. FURTHER INVESTIGATION FOUND DAMAGE MICROPROCESSOR UNIT BOARD, INTERNAL REAL |
| Source | openFDA MAUDE (device adverse events) |
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