GE Healthcare · X-ray R&F
AMX3 - FDA Knob Recall The customer found an obscure FDA recall.
AMX3 - FDA Knob Recall
Symptom
AMX3 - FDA Knob Recall The customer found an obscure FDA recall. It involved the operator knobs on the AMX 3. The knobs if not properly put on could make an incorrect technique setting.
Applies to
- Product
- Portables
- Component
- AMX110 AMX2 AMX3
- Area
- X-ray R&F
Full cause & step-by-step resolution
The complete cause analysis, the step-by-step remedy for this GE Healthcare X-ray R&F issue are available to FSELIB subscribers — re-authored, web-first, searchable.
7-day free trial · no credit card required
Related GE Healthcare X-ray R&F issues
- ADx-E Advantx-E console displayed a 6C00 Error (Digital Imaging Subsystem error - Error status received in IDC Prep Reply) when the first exposure of detector bad pixel calibration was attempted; cali…
- AEC Backup Time message
- New style ion chamber does not have a preamp
- Precision 500D Table Fluoro Carriage Front Bumper is not properly adjusted, allows excessive travel toward the front of the table.
- Precision 500D Aurora, dose readout does not update when an overhead Rad Tube Exposure is made, at any technic due to abnormally low mR/mAS from the Rad Overhead XRT.
- P500D Aurora with M4 Software (May 2006 Release), Dose Readout Correct on Console, Dose Printer Prints 0.0 due to a M4 Software Bug