FOLFUSOR Adverse Event — Malfunction (MDR 1416980-2020-02382)
FOLFUSOR Adverse Event — Malfunction (MDR 1416980-2020-02382) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: FOLFUSOR; Generic name: PUMP, INFUSION, ELASTOMERIC; Manufacturer: BAXTER HEALTHCARE CORPORATION.
| Device | FOLFUSOR |
|---|---|
| Generic name | PUMP, INFUSION, ELASTOMERIC |
| Manufacturer | BAXTER HEALTHCARE CORPORATION |
| Report number | 1416980-2020-02382 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, CONSUM |
| Narrative | (B)(6). SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. |
| Source | openFDA MAUDE (device adverse events) |
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