CADD Adverse Event — Malfunction (MDR 3012307300-2020-03401)
CADD Adverse Event — Malfunction (MDR 3012307300-2020-03401) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CADD; Generic name: SOLIS, VIP; Manufacturer: SMITHS MEDICAL ASD, INC..
| Device | CADD |
|---|---|
| Generic name | SOLIS, VIP |
| Manufacturer | SMITHS MEDICAL ASD, INC. |
| Report number | 3012307300-2020-03401 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | USER FACILITY |
| Narrative | INFORMATION WAS RECEIVED THAT DEVICE IS UNDER DOSING BY SIX PERCENT. NO ADVERSE EFFECTS REPORTED. |
| Source | openFDA MAUDE (device adverse events) |
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