FDA Adverse Event
Other
Summary report: N
9613347-2005-00037
MDR report key: 966518
·
Received July 14, 2006
Report
- Report Number
- 9613347-2005-00037
- Event Type
- Other
- Date Received
- July 14, 2006
- Product Code
- FFK
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
OUR SERVICE TECH COULD NOT DUPLICATE THE PROBLEM AND DECIDED TO REPLACE THE BASIC MOTION CONTROL BOARD TO ELIMINATE THE POSSIBLE SOURCE OF THE PROBLEM. THE CONTROL PANEL CONNECTION HAD INDICATION OF ARCING WHICH COULD BE CAUSED FROM THE OPERATOR PLUGGING OR UNPLUGGING THE CONNECTION INTO THE TABLE WHILE THE TABLE IS POWERED UP. THE OPERATOR WAS CAUTIONED AGAINST THIS PRACTICE. THE CONTROL PANEL IS REPLACED AS WELL.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | FFK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |