CADD MS3 PUMP Adverse Event — Malfunction (MDR 3012307300-2020-03410)
CADD MS3 PUMP Adverse Event — Malfunction (MDR 3012307300-2020-03410) 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 | 3012307300-2020-03410 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | DISTRIBUTOR |
| Narrative | DEVICE EVALUATION: ONE CADD MS3 PUMP WAS RETURNED FOR ANALYSIS DUE TO LOSS IN PROGRAMMING. FUNCTIONAL AND VISUAL TESTING WAS PERFORMED. THE ISSUE WAS NO DUPLICATED. TESTING WAS PERFORMED AND THE DEVICE DID NOT LOSE ANY PROGRAM. THE DEVICE RAN THE PROGRAM FOR AN EXTENDED PERIOD OF TIME WITH NO ISSUES OCCURRING. THEREFORE, NO PROBLEM FOUND WITH THE ISSUE. |
| Source | openFDA MAUDE (device adverse events) |
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