Toshiba · Model PowerVision 8000
512 channels, Wideband Imaging Electronic Convex, Linear, and Sector Scanning Three Transducer Selection Switch, and CW connector Transducers Triplex Capable 15" High Resolution Color Monitor Touch Command Screen (TCS) Cine Loop, B-Mode, M-Mode PW, and CW Doppler Color Doppler (both B-Mode and M-Mode) Tissue Harmonic Imaging (THI) Selectable Doppler Frequency Directory and Memory for 250 Patients
Failure patterns typical of this equipment class - general BMET reference, not verified against this exact unit's own service history unless flagged. Severity is a category-level estimate.
Symptoms: Dropout, dead elements, image banding.
Root cause: Element delamination or cable damage from repeated use.
Symptoms: Intermittent image loss, connector-wiggle artifact.
Root cause: Repeated flexing and connector strain.
Symptoms: Frozen console, acquisition timeout.
Root cause: Workstation or storage degradation.
Symptoms: Dim image, color shift, dead pixels.
Root cause: Backlight or LCD panel aging.
The parts a BMET typically services on this class of equipment. Service class and relative cost are general engineering estimates for the category, not figures from this unit's documentation. Part numbers appear only when pulled from this unit's own service manual. Always confirm intervals and pricing against the manufacturer.
Handle with care; most-replaced probe assembly.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Transducer cable assembly | Periodic replacement | $$ | Fairly easy |
| Workstation / GPU | Periodic replacement | $$$ | Difficult |
| Display panel | Major service part | $$ | Moderate |
| Ultrasound transducer / probe Handle with care; most-replaced probe assembly. | Periodic replacement | $$$$ | Moderate |
Relative cost: $ lowest · $$$$ 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 structured starting point derived from the failure modes above. 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.
No documents available for this device yet.
Synced live from the FDA openFDA API.
The recall was initiated because Toshiba has confirmed that during patient transfer from a gurney to the catherization table, the tabletop may rotate unexpectedly when sufficient force is applied to the tabletop. The result of the tabletop rotating unexpectedly is the patient being tranferred may fall from the tabletop.
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