Stryker 596T Console Unit
Stryker · Model 596T Console Unit
Stryker 596T Camera Console Unit.
Key tips
- ·A failed leak test means the scope does not get reprocessed or used - send it for repair, full stop.
- ·A shortened reprocessing cycle is a real infection-control failure, not a minor deviation - follow AAMI ST91 exactly.
- ·Track light-source lamp-hours against the manufacturer's limit rather than running to failure.
Typical Failure Modes
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.
No or dim illumination / lamp fault
HighSymptoms: No light output, dim or flickering light, lamp-hours alarm, colour shift.
Root cause: Xenon / LED lamp at end of life, a lamp power supply fault, or a light-cable fault.
Poor video image
HighSymptoms: Noisy, dark, discoloured or out-of-focus image, dropouts, no image.
Root cause: Camera head / coupler fault, a camera-cable fault, or a CCU / video-processor fault.
White-balance / colour fault
MediumSymptoms: Cannot white-balance, persistent colour cast.
Root cause: Camera head sensor drift, a dirty coupler, or the light source colour temperature.
Overheating / fan fault
LowSymptoms: Thermal shutdown, loud fan, hot exhaust.
Root cause: Failed or clogged cooling fan.
Output / connector fault
LowSymptoms: Signal only on one output, connector damage, HD/SDI dropout.
Root cause: Worn video output connector or an output board fault.
Serviceable Parts & Consumables
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.
Xenon / LED lamp module
Class Frequent wear itemRel. cost $$$R&R Fairly easy
Camera head / coupler
Class Periodic replacementRel. cost $$$R&R Moderate
Camera cable
Class Periodic replacementRel. cost $$R&R Fairly easy
Fibre-optic light cable
Class Periodic replacementRel. cost $$R&R Easy
CCU / video-processor board
Class Major service partRel. cost $$$R&R Difficult
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Xenon / LED lamp module | Frequent wear item | $$$ | Fairly easy |
| Camera head / coupler | Periodic replacement | $$$ | Moderate |
| Camera cable | Periodic replacement | $$ | Fairly easy |
| Fibre-optic light cable | Periodic replacement | $$ | Easy |
| CCU / video-processor board | Major service part | $$$ | Difficult |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
PM Checklist
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.
- ·Leak testing before each reprocessing cycle
- ·Scope reprocessing per AAMI ST91
- ·Light source lamp-hour tracking
- ·Annual full PM
Troubleshooting Approach
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.
Symptom: No or dim light
- Check the lamp-hours counter and replace the lamp module if near / past its rating.
- Inspect the fibre-optic light cable for dark (broken) fibres against a bright light.
- Confirm the lamp strikes (listen / watch) and the fan runs.
- Replace the lamp power supply if the lamp will not strike.
- Verify full brightness with a fresh cable.
Symptom: Poor video image
- Clean the scope lens and coupler and re-white-balance.
- Swap the camera head and cable to isolate head vs CCU.
- Confirm the light source output and cable.
- Try a second monitor / output cable.
- Replace the camera head or refer the CCU as isolated.
Typical Location
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
- Endoscopy suite / GI lab
- Operating Room
- Bronchoscopy suite
Documents & Manuals
No documents available for this device yet.
Safety & Recalls
Synced live from the FDA openFDA API.
- RECALL
Unreleased software was installed on customer systems resulting in the visual feedback on the screen to show the points to be off from the physical reference point of the pointer or suction.
- RECALL
A software defect in the camera control unit (CCU) will cause the image on the monitor to flip upside-down into an incorrect orientation. The potential of harms are conversion to open procedure, additional medical intervention, or a revision surgery.
- RECALL
The device could have a missing spanner nut and snap ring which could potentially result in the equipment falling.
- RECALL
The firm received complaints regarding insufficient irrigation to the tip of the Sonopet system. Lack of irrigation can potentially lead to excessive heat at the tip.
- RECALL
Stryker Instruments is voluntarily recalling the single use 2.5MM Aggressive Blade because the line on the affected part (P/N 5290-928-000, Lot #13280CG2) was a straight line without a number scale or logo. The line required for this part number includes a number scale that goes from 1cm 7cm.
- RECALL
Stryker received reports from the field of the impaction plate dissociating/fracturing from the main body of the broach handle.
- RECALL
A supplied component exhibiting corrosion was built into the power supply boards of the Sonopet Consoles listed above. The issue is limited to 2 lots of the supplied component. The presence of the corrosion on the relay of the power supply board can potentially lead to a conduction defect which could cause the irrigation pump to stop working. The purpose of the irrigation pump is to supply sali
- RECALL
Product may not adequately visualize IR light emitted from U- and E- kits due to a manufacturing error.
- RECALL
RF energy or powered shaver handpieces may continue to operate when not intended when used with the iSwitch Wireless Foot switch.
- RECALL
On 06/09/2009, Stryker Sustain ability Solutions, formerly Ascent Healthcare Solutions, recalled lots 674201 & 674290 of their Reprocessed Mitek Arthroscopic Wand due to the lots not being tested in accordance with the functional test requirement during the time frame of 04/14/09 to 05/25/09.
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