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
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.
Print head / thermal head wear
HighSymptoms: Streaking, missing lines, or degraded print quality.
Root cause: Thermal head element wear from print-cycle count.
Media jam / feed fault
MediumSymptoms: Paper, film, or media misfeed or jam mid-print.
Root cause: Worn feed rollers or debris in the media path.
Network / driver connectivity fault
MediumSymptoms: Won't receive print jobs from the connected workstation or modality.
Root cause: Network configuration, driver, or interface card fault.
Ribbon / ink / toner depletion
LowSymptoms: Faded, streaked, or blank output.
Root cause: Consumable exhausted or improperly seated.
Serviceable Parts & Consumables
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.
Print head / thermal head assembly
Class Periodic replacementRel. cost $$$R&R Moderate
Ribbon / ink or toner cartridge
Consumable - replace per print-volume schedule.
Class ConsumableRel. cost $R&R Easy
Media feed roller set
Class Periodic replacementRel. cost $$R&R Fairly easy
Network interface / driver board
Class Major service partRel. cost $$$R&R Moderate
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Print head / thermal head assembly | Periodic replacement | $$$ | Moderate |
| Ribbon / ink or toner cartridge Consumable - replace per print-volume schedule. | Consumable | $ | Easy |
| Media feed roller set | Periodic replacement | $$ | Fairly easy |
| Network interface / driver board | Major service part | $$$ | Moderate |
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 structured starting point derived from the failure modes above. Follow the manufacturer's service documentation for the actual procedure.
Symptom: Print head / thermal head wear
- Confirm the presentation - typically streaking, missing lines, or degraded print quality.
- Check the most likely cause first: thermal head element wear from print-cycle count.
- Inspect the affected subsystem against the manufacturer's inspection checklist.
- If the fault is confirmed and not a field adjustment, service or replace the print head / thermal head assembly per the manufacturer's service documentation.
- Return the device to service only after the manufacturer's functional and applicable electrical-safety checks pass.
- Record the findings, any parts used, and the verification results in the maintenance history.
Symptom: Media jam / feed fault
- Confirm the presentation - typically paper, film, or media misfeed or jam mid-print.
- Check the most likely cause first: worn feed rollers or debris in the media path.
- Inspect the affected subsystem against the manufacturer's inspection checklist.
- If the fault is confirmed and not a field adjustment, service or replace the ribbon / ink or toner cartridge per the manufacturer's service documentation.
- Return the device to service only after the manufacturer's functional and applicable electrical-safety checks pass.
- Record the findings, any parts used, and the verification results in the maintenance history.
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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