Stryker 240-010-400
Stryker · Model 240-010-400
Stryker Endoscopy Mega High Definition Printer Stryker EndoscopyMega High Definition Printer.
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.
Poor print quality
HighSymptoms: Density too light / dark, banding, streaks, non-uniform image, blotches.
Root cause: Print head / laser optics contamination, film / cartridge issue, or density-calibration drift.
Film jam / transport fault
MediumSymptoms: Film jams in the pick-up or transport, mis-feeds, or multi-feeds.
Root cause: Worn pick-up rollers, a transport-roller fault, or a mis-loaded film cartridge.
Density / calibration fault
MediumSymptoms: Prints do not match the reference, calibration fails, densitometer error.
Root cause: Internal densitometer or the calibration routine.
DICOM / queue fault
MediumSymptoms: Jobs stuck in the queue, printer offline to modalities, association failures.
Root cause: Network / DICOM configuration or the controller board.
Thermal head / laser fault
MediumSymptoms: Whole-image defect, print-engine error.
Root cause: Thermal print head or the laser / optics module.
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.
Pick-up / transport rollers
Class Periodic replacementRel. cost $$R&R Moderate
Thermal print head / laser optics
Class Periodic replacementRel. cost $$$R&R Difficult
Internal densitometer
Class Major service partRel. cost $$R&R Moderate
Controller / network board
Class Major service partRel. cost $$R&R Moderate
Film (media)
Class ConsumableRel. cost $$R&R Easy
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Pick-up / transport rollers | Periodic replacement | $$ | Moderate |
| Thermal print head / laser optics | Periodic replacement | $$$ | Difficult |
| Internal densitometer | Major service part | $$ | Moderate |
| Controller / network board | Major service part | $$ | Moderate |
| Film (media) | Consumable | $$ | Easy |
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: Poor print quality
- Print the built-in test / SMPTE pattern.
- Run the density calibration.
- Clean the print head / laser optics per the manual.
- Confirm the film type / cartridge matches the printer setting.
- Replace the print head or optics module if a whole-image defect persists.
Symptom: Film jam or jobs stuck
- Clear the jam and note the location.
- Inspect and clean the pick-up and transport rollers.
- For queue problems, check the DICOM association and network.
- Restart the print controller.
- Send a test job from a modality to confirm.
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
An error was identified on the expiration date of the product label. The shelf life for the products impacted is 36 months (3 years) however the product label represents a 54 month (4.5 year) shelf life.
- RECALL
Stryker has identified a nonconformance in specific lots of Hoffmann LRF Bone Transport Struts. Specifically, the thread pitch is oversized at the distal end of the threaded rod, and as a result the distal ring fixation cannot be locked between 0- 50mm of the threaded rod.
- RECALL
During a review of the packaging, it was determined that the seal integrity of the pouch may be decreased.
- RECALL
The electrical cord power plug design may allow the prongs to develop a fracture inside or outside the plug, if the plug is misused.
- RECALL
The pump may display an E-4 error message, which causes the pump to stop dispensing the pain medication.
- RECALL
Mis-labeling; The instructions for use include a use for which the device is not intended. (Device not approved to capture a bone biopsy)
- RECALL
Product package may crack and cause loss of sterility.
- RECALL
Slider Lock Failure - The ACL Workstation slider, a component of the ACL workstation, does not consistently lock into the ACL Workstation Base.
- RECALL
The bubble in a vial of the Pelvic Alignment Level (PAL) was wider than the level marking. Upon opening the PAL and removing the vial, it was discovered that the vial was leaking
- RECALL
Lack of Labeling Precautions. Calstrux should not be used in combination with other products and the volume used should approximate the size of the defect. Adverse reactions have been reported with over filling the defect site or combination product usage, including localized induration, swelling, inflammation, wound drainage, infection and device migration.
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