SPECTRUM INFUSION IQ PUMP Adverse Event — Malfunction (MDR 1314492-2020-01408)
SPECTRUM INFUSION IQ PUMP Adverse Event — Malfunction (MDR 1314492-2020-01408) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SPECTRUM INFUSION IQ PUMP; Generic name: INFUSION PUMP; Manufacturer: BAXTER HEALTHCARE CORPORATION.
| Device | SPECTRUM INFUSION IQ PUMP |
|---|---|
| Generic name | INFUSION PUMP |
| Manufacturer | BAXTER HEALTHCARE CORPORATION |
| Report number | 1314492-2020-01408 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, HEALTH |
| Narrative | ADDITIONAL INFORMATION H3, H6 AND H10: BAXTER RECEIVED AND EVALUATED THE DEVICE. VISUAL INSPECTION DID NOT IDENTIFY ANY ABNORMALITIES THAT COULD HAVE CONTRIBUTED TO THE REPORTED CONDITION. A DEVICE HISTORY REVIEW REVEALED NO ISSUES THAT COULD HAVE CAUSED OR CONTRIBUTED TO THE REPORTED ISSUE. THE REPORTED CONDITION WAS NOT VERIFIED. THE EVENT HISTORY LOG (EHL) REVIEW WAS PERFORMED AND REVEALED THAT |
| Source | openFDA MAUDE (device adverse events) |
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