ALARIS® PUMP MODULE Adverse Event — Malfunction (MDR 2016493-2020-00563)
ALARIS® PUMP MODULE Adverse Event — Malfunction (MDR 2016493-2020-00563) 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 | 2016493-2020-00563 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE, HEALTH |
| Narrative | NO DEVICE WILL BE RETURNED PER CUSTOMER. THE CUSTOMER COMPLAINT COULD NOT BE CONFIRMED BECAUSE THE DEVICE WAS NOT SEQUESTERED FOR FAILURE INVESTIGATION. THE ROOT CAUSE OF THIS FAILURE WAS NOT IDENTIFIED. |
| Source | openFDA MAUDE (device adverse events) |
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