FLOGARD Adverse Event — Malfunction (MDR 1416980-2020-02403)
FLOGARD Adverse Event — Malfunction (MDR 1416980-2020-02403) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: FLOGARD; Generic name: PUMP, INFUSION; Manufacturer: BAXTER HEALTHCARE CORPORATION.
| Device | FLOGARD |
|---|---|
| Generic name | PUMP, INFUSION |
| Manufacturer | BAXTER HEALTHCARE CORPORATION |
| Report number | 1416980-2020-02403 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, HEALTH |
| Narrative | THE DEVICE WAS NOT RETURNED; THEREFORE, A DEVICE ANALYSIS COULD NOT BE COMPLETED. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. |
| Source | openFDA MAUDE (device adverse events) |
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