NI Adverse Event — Malfunction (MDR 1416980-2020-02417)
NI Adverse Event — Malfunction (MDR 1416980-2020-02417) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: NI; Generic name: SET, I.V. FLUID TRANSFER; Manufacturer: BAXTER HEALTHCARE CORPORATION.
| Device | NI |
|---|---|
| Generic name | SET, I.V. FLUID TRANSFER |
| Manufacturer | BAXTER HEALTHCARE CORPORATION |
| Report number | 1416980-2020-02417 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE |
| Narrative | THE DEVICE WAS NOT RETURNED AND THE LOT NUMBER IS UNKNOWN; 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) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →