SPECTRUM INFUSION PUMP Adverse Event — Malfunction (MDR 1314492-2020-01419)
SPECTRUM INFUSION PUMP Adverse Event — Malfunction (MDR 1314492-2020-01419) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SPECTRUM INFUSION PUMP; Generic name: INFUSION PUMP; Manufacturer: BAXTER HEALTHCARE CORPORATION.
| Device | SPECTRUM INFUSION PUMP |
|---|---|
| Generic name | INFUSION PUMP |
| Manufacturer | BAXTER HEALTHCARE CORPORATION |
| Report number | 1314492-2020-01419 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE, HEALTH |
| Narrative | THE DEVICE WAS RECEIVED, AND AN EVALUATION IS COMPLETE. THE DEVICE RECEIVED INCOMING DEVICE EVALUATION ASSESSMENT (IDEA). THIS EVALUATION INCLUDED A VISUAL ASSESSMENT AS WELL AS FUNCTIONAL TESTING. THE DEVICE FAILED IDEA TESTING DUE TO AN AIR IN LINE ERROR. A DEVICE HISTORY RECORD REVIEW REVEALED NO ISSUES THAT COULD HAVE CAUSED OR CONTRIBUTED TO THE EVENT. SERVICE EVALUATION VERIFIED THE AIR IN L |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →