ALARIS® PUMP MODULE Adverse Event — Malfunction (MDR 2016493-2020-00571)
ALARIS® PUMP MODULE Adverse Event — Malfunction (MDR 2016493-2020-00571) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ALARIS® PUMP MODULE; Generic name: PUMP, INFUSION; Manufacturer: CAREFUSION.
| Device | ALARIS® PUMP MODULE |
|---|---|
| Generic name | PUMP, INFUSION |
| Manufacturer | CAREFUSION |
| Report number | 2016493-2020-00571 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE, OTHER |
| Narrative | CORRECTION: DISREGARD FILE (AFTER FURTHER REVIEW, FILE IS REVISED TO NOT-REPORTABLE AS THERE IS NO ALLEGATION OF OVER/UNDER OR FREE FLOW EVENTS, AS WELL AS PATIENT INVOLVEMENT.) |
| Source | openFDA MAUDE (device adverse events) |
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