Stryker 240-010-194
Stryker · Model 240-010-194
Stryker Endoscopy Model High Definition Color 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.
Media feed roller set
Class Periodic replacementRel. cost $$R&R Fairly easy
Network interface / driver board
Class Major service partRel. cost $$$R&R Moderate
Print head / thermal head assembly
Class Periodic replacementRel. cost $$$R&R Moderate
Ribbon / ink or toner cartridge
Consumable - replace per print-volume schedule.
Class ConsumableRel. cost $R&R Easy
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Media feed roller set | Periodic replacement | $$ | Fairly easy |
| Network interface / driver board | Major service part | $$$ | Moderate |
| Print head / thermal head assembly | Periodic replacement | $$$ | Moderate |
| Ribbon / ink or toner cartridge Consumable - replace per print-volume schedule. | 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 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
There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.
- 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 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.
- RECALL
The press fit connection of the Angular Sleeve and pin of the U-Joint and Click Lock did not meet specification. A dimensional discrepancy of the bore hole of the Angular Sleeve may cause a reduced press fit of the pin. This can result in partial of full displacement or loss of the pin and, accordingly, stability of the strut of the frame cannot be ensured.
- 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
Instruction for use incorrect: There are no statements or warning on labels or Instructions for Use that 8, 9 and 10 mm diameter MRS Cemented Stems are indicated only for use in the GMRS Proximal Tibial and Distal Femoral Components.
- 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.
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