ALARIS PUMP MODULE Adverse Event — Malfunction (MDR 2016493-2020-00595)
ALARIS PUMP MODULE Adverse Event — Malfunction (MDR 2016493-2020-00595) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ALARIS PUMP MODULE; Generic name: PUMP, INFUSION; Manufacturer: CAREFUSION SD.
| Device | ALARIS PUMP MODULE |
|---|---|
| Generic name | PUMP, INFUSION |
| Manufacturer | CAREFUSION SD |
| Report number | 2016493-2020-00595 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | FOREIGN, OTHER |
| Narrative | THE AFFECTED PRODUCT HAS BEEN RECEIVED AND THE INVESTIGATION IS PENDING. A FOLLOW UP REPORT WILL BE SUBMITTED ONCE THE FAILURE INVESTIGATION HAS BEEN COMPLETED. AS PREVIOUSLY DISCUSSED WITH THE CUSTOMER, IT IS THEIR POLICY NOT TO PROVIDE PATIENT DEMOGRAPHICS. |
| Source | openFDA MAUDE (device adverse events) |
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