ALARIS® PUMP MODULE Adverse Event — Malfunction (MDR 2016493-2020-00554)
ALARIS® PUMP MODULE Adverse Event — Malfunction (MDR 2016493-2020-00554) 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 | 2016493-2020-00554 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE, OTHER |
| Narrative | NO PRODUCT RETURNED. BECAUSE NO DEVICE OR DEVICE LOGS WERE RETURNED OR EXPECTED TO BE RETURNED, NO FAILURE INVESTIGATION COULD BE PERFORMED. THE ROOT CAUSE OF THE CUSTOMER'S EXPERIENCE WAS NOT IDENTIFIED. |
| Source | openFDA MAUDE (device adverse events) |
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