AIA-2000 Adverse Event — Malfunction (MDR 8031673-2020-00126)
AIA-2000 Adverse Event — Malfunction (MDR 8031673-2020-00126) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: AIA-2000; Generic name: AIA-2000; Manufacturer: TOSOH CORPORATION.
| Device | AIA-2000 |
|---|---|
| Generic name | AIA-2000 |
| Manufacturer | TOSOH CORPORATION |
| Report number | 8031673-2020-00126 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | HEALTH PROFESSIONAL |
| Narrative | A FIELD SERVICE ENGINEERING (FSE) WAS AT THE CUSTOMER'S SITE TO ADDRESS REPORTED EVENT. FSE CONFIRMED ERROR BY REVIEWING ERROR LOGS AND REPRODUCED THE REPORTED ERROR BY ATTEMPTING TO PERFORM A BF PROBE WASH RUN. WHILE TROUBLESHOOTING, FSE FOUND DRIED UP WASH ON THE SENSOR AND ALSO THE AXIS SCREW WAS DIRTY. FSE CLEANED THE SENOR TO THE PROBE ALSO CLEANED AND LUBRICATED THE AXIS SCREW TO PROBE 3. FS |
| Source | openFDA MAUDE (device adverse events) |
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