ULTRA MINIBORE EXTENSION SET Adverse Event — Malfunction (MDR 9616066-2020-01503)
ULTRA MINIBORE EXTENSION SET Adverse Event — Malfunction (MDR 9616066-2020-01503) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ULTRA MINIBORE EXTENSION SET; Generic name: SET, ADMINISTRATION, INTRAVASCULAR; Manufacturer: CAREFUSION.
| Device | ULTRA MINIBORE EXTENSION SET |
|---|---|
| Generic name | SET, ADMINISTRATION, INTRAVASCULAR |
| Manufacturer | CAREFUSION |
| Report number | 9616066-2020-01503 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, OTHER |
| Narrative | THE AFFECTED PRODUCT HAS BEEN RECEIVED AND THE INVESTIGATION IS PENDING. A FOLLOW UP REPORT WILL BE SUBMITTED ONCE THE FAILURE INVESTIGATION HAS BEEN COMPLETED. |
| Source | openFDA MAUDE (device adverse events) |
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