ALARIS PUMP MODULE Adverse Event — Malfunction (MDR 2016493-2020-00608)
ALARIS PUMP MODULE Adverse Event — Malfunction (MDR 2016493-2020-00608) 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 | 2016493-2020-00608 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, HEALTH |
| Narrative | NO DEVICE WILL BE RETURNED PER CUSTOMER. THE CUSTOMER DECLINED TO RETURN THE DEVICE FOR FAILURE INVESTIGATION. THE ROOT CAUSE OF THIS FAILURE WAS NOT IDENTIFIED. |
| Source | openFDA MAUDE (device adverse events) |
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