Stryker · Model Vision Flat Panel Monitor
Stryker Vision Flat Panel Monitor
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: Dead pixels, backlight failure, or no image at all.
Root cause: LCD/LED panel or backlight driver aging.
Symptoms: No signal, wrong input source, or image artifacts.
Root cause: Input board, cable, or connector fault.
Symptoms: Won't power on, intermittent shutdown.
Root cause: Internal power supply module aging.
Symptoms: Unresponsive touch, drifting calibration.
Root cause: Touch overlay or controller board wear.
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.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Touch panel overlay | Periodic replacement | $$ | Fairly easy |
| Power supply module | Periodic replacement | $$ | Fairly easy |
| Display panel / backlight assembly | Major service part | $$$$ | Difficult |
| Video input board | Major service part | $$ | Fairly easy |
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 mounts on the monitor may have an insufficient weld.
Stryker C2 NerveMonitor's design and instructions may not optimally address usability issues related to the functionality of the device, which may result in use errors potentially causing or contributing to nerve injury.
The mounts on the monitor may have an insufficient (missing or incomplete) weld.
An incorrect sterility status on the label, non-sterile products labeled as sterile
Stryker Orthopaedics has received two customer complaints regarding Duracon Tibial Wedge implants puncturing the packaging's Tyvek lid(s).
Stryker has initiated the recall of its Aria Standard and Specialty Implant Inserters due to complaints of product fracturing.
During the use of the SHAPE Arm there is the potential for the monitor mount to come off of the SHAPE Arm if the lock washer and screw are not present.
Stryker has received complaints from customers relating to fracture along the weld that binds the handle to the shaft of the static inserter.
When positioning the display located on top of the video cart, it is possible for the user to apply excessive force and push the display up and out of the mounting arm. This can result in the display falling upon the user/patient.
Stryker has become aware that there is a low likelihood of incomplete engagement of the Spring Arm Circlip during service or replacement of the Spring Arm. If the Spring Arm Circlip is not fully seated, the Spring Arm could separate and fall along with the surgical lights or monitors mounted to the end of the Spring Arm. To date, there have been no serious injuries reported from the incomplete e
The firm identified two complaints have been reported indicating that the product inside the package did not match with the label information. The product was labeled as Flat Proximal Pressurizer P/N 0206-556-000 while the product inside the package was Femoral Pressurizer P/N 0206-566-000.
Some of the pitch shafts were not properly welded which results in the monitor becoming unlevel.
Knob parts stick together, resulting in poor functionality of the knob.
Circlip component used to suspend flat panel and navigation arm system may become dislodged.
Paint chips: Shroud used to cover cables on the Stryker Vision 3 flat panel monitor (monitor used in surgery rooms during procedures) was not manufactured/painted to specification, resulting in the possibility that paint chips could fall off and fall into non-sterile and/or sterile fields during surgery. For further information, please contact Stryker Communications Corporation by telephone at 97
The pressure indicated may be inaccurate, and this inaccuracy may be not detectable by the user.
Certain sterile packed drills with center tip may penetrate the foam and blister resulting in loss of sterility.
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