CADD MS3 PUMP Adverse Event — Malfunction (MDR 3012307300-2020-03413)
CADD MS3 PUMP Adverse Event — Malfunction (MDR 3012307300-2020-03413) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CADD MS3 PUMP; Generic name: PUMP, INFUSION; Manufacturer: ST PAUL.
| Device | CADD MS3 PUMP |
|---|---|
| Generic name | PUMP, INFUSION |
| Manufacturer | ST PAUL |
| Report number | 3012307300-2020-03413 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | DISTRIBUTOR |
| Narrative | IT WAS REPORTED THAT THE SMITHS MEDICAL CADD MS3 PUMP HAD LOST PROGRAMMING DUE TO NO BATTERY CHANGE. REPORTER STATED THAT THERE WAS NO PATIENT INVOLVEMENT IN THE REPORTED EVENT. |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →