
Toshiba · Model Aplio 500
Ultrasound System The Aplio 500 Platinum system features industry-first imaging and visualization capabilities and delivers exceptional image quality to sophisticated ergonomics that elevate efficiency to the highest levels. Delivers outstanding performance for superior clinical precision, diagnostic confidence and departmental productivity. The system features a proprietary 2D Wall Motion Tracking technology, which provides stunning visualization and quantitative analysis of cardiac function with accuracy and reproducibility.
Compiled for this model from its own documentation and established engineering knowledge for this equipment class - not from a verified service record. Confirm against the manufacturer's service manual.
Symptoms: Noisy, low-contrast or non-uniform image, missing sector, drop-out that follows the system not the probe.
Root cause: Front-end / beamformer board fault, a probe-port (connector) board fault, or a system-board fault.
Symptoms: A probe works on one port but not another, or is not detected at all.
Root cause: Worn probe-port connector or a scan-connector board fault.
Symptoms: Dead system, hangs at boot, or powers off under load.
Root cause: Power supply / DC converter, the system battery, or a system-board fault.
Symptoms: Unresponsive TGC sliders or keys, distorted or blank display.
Root cause: Control-panel board, touchscreen, or the monitor.
Symptoms: Thermal-shutdown warning, fan roar, hot exhaust.
Root cause: Failed or dust-clogged cooling fan or blocked air path.
Symptoms: Studies will not send to PACS, images will not archive, worklist empty.
Root cause: Network configuration or a storage-drive fault.
Serviceable items for this model, compiled from its documentation and engineering knowledge for this equipment class. Service class and relative cost are estimates, not manufacturer figures; no part numbers are given. Confirm intervals and pricing against the manufacturer.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Front-end / beamformer board | Major service part | $$$$ | Difficult |
| Probe-port / scan-connector board | Major service part | $$$ | Difficult |
| Power supply / DC converter | Major service part | $$$ | Difficult |
| Control-panel / touchscreen assembly | Major service part | $$$ | Moderate |
| Cooling fan | Major service part | $ | Moderate |
| System hard drive | Major service part | $$ | Moderate |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
Preventive-maintenance tasks typical of this equipment class. Perform to the manufacturer's procedure and your facility's policy - this is general reference, not a schedule for this specific unit.
A starting sequence for this model, compiled from its documentation and engineering knowledge for this equipment class. Follow the manufacturer's service documentation for the actual procedure.
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
Synced live from the FDA openFDA API.
The power supply unit may be damaged and may fail to start up when the power plug is inserted into a power outlet while the main power switch on the rear of the system is set to ON.
Toshiba Medical Systems has received reports of startup issues with the Toshiba TUS-500 and TUS-300 ultrasound systems. The startup issue is predominant when attempting to bring the system up from standby mode when the system is used remotely. It has been determined that this may potentially cause damage to the system.
Toshiba America Medical Systems, Inc. is initiating a field correction on the Aplio Artida Ultrasound Diagnostic System because the panel operation for the Aplio Artida may become disabled (i.e., system may hang up) when processing to display patient information (heart rate, time, VCP counter, ect.).
Toshiba America Medical Systems is initiating a field correction on the SSH-880CV Aplio Artida Diagnostic Ultrasound System due to software issues.
Toshiba America Medical Systems Inc (TAMS) is initiating a field correction on the the Aplio XG model SSA-790A because it did not meet the requirement of clause 15b, IEC60601-1 which requires that the residual voltage shall not exceed 60V after 1 second from taking off the AC plug.
There is a possibility of the system shutting down owing to the power supply unit causing the protection function to activate thus turning off the system prematurely.
Toshiba America Medical Systems (TAMS) has become aware that the FLEX M software has reversed left and right annotation and post FLEX M measurement error, which may result in incorrect values.
Toshiba America Medical Systems is initiating a field correction on the PVT-681MV Endocavitary Transducer used with the Aplio XG and Xario XG Ultrasound Systems due to an incorrect sweep direction setting. Images acquired using the endo-cavitary transducer PVT-681MV and cross-sectional images created from these volume images are reversed horizontally on the Aplio XG (SSA-790A) and the Xario XG (
Toshiba America Medical Systems (TAMS) is initiating a field correction on the SSH-880CV Aplio Artida System due to a problem related to a wrong measurement value display in using with DICOM viewer. When an image is transferred from this system in DICOM transfer and a measurement is performed on a Doppler image in the DICOM viewer, measured values such as VTI (Velocity Time Integral) and PI/RI
Toshiba America Medical System Inc initiated a field corrective action on Aplio 50; SSA-700A; software version 5.5r002 and later, Aplio 80; SSA-700A; software version 5.5r002 and later, and Xario; SSA-660A; software version 1.0 and later, because the product does not meet the Safety Standard requirements.
Panel Lock-up: When using dynamic image acquisition modes the panel may lock up, if the operator attempts to perform a still image capture. If the panel locks up the system will have to be rebooted to continue the examination which may cause a delay in completion of the patient examination.
When using the LV measurement function and making numerous measurements the value displayed on the image screen may on occasion not update correctly. The values that are stored in MDA (measurement display area) are correct and no issue has been reported with these values.
If the measurement mode is started from the Doppler mode and then the sweep speed setting is changed by the assigned user function, the measurement of the time direction results don't correspond to the actual values.
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