CADD Adverse Event — Malfunction (MDR 3012307300-2020-03429)
CADD Adverse Event — Malfunction (MDR 3012307300-2020-03429) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CADD; Manufacturer: SMITHS MEDICAL ASD, INC.; Report number: 3012307300-2020-03429.
| Device | CADD |
|---|---|
| Manufacturer | SMITHS MEDICAL ASD, INC. |
| Report number | 3012307300-2020-03429 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | USER FACILITY |
| Narrative | INFORMATION WAS RECEIVED INDICATING THAT A SMITHS MEDICAL PUMP HAS FAILED THE VOLUME TEST. THERE WAS NO PATIENT PRESENT AT THE TIME OF THE EVENT. THERE WERE NO REPORTED ADVERSE EVENTS REPORTED. |
| Source | openFDA MAUDE (device adverse events) |
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