Stryker 570 Camera Head
Stryker · Model 570 Camera Head
Stryker 570 Camera Head is classified as Camera (Endoscopy). No manufacturer description has been sourced for this model yet.
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
Expired Products distributed to customers
- RECALL
There is potential the device inside the package may not match the product information on the outer label (e.g., label states 5820-107-030 but package contains a 5820-107-530 device).
- RECALL
There is potential the device inside the package may not match the product information on the outer label (e.g., label states 5820-107-430 but package contains a 5820-107-530 device or vice versa).
- 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
Stryker Instruments is voluntarily recalling specific lots of sterile MIS Toolsteel Burs because the burs may exhibit signs of corrosion.
- RECALL
Stryker received several complaints describing incidence of harm secondary to taper lock failure for specific lots of numerous catalog numbers of LFIT Anatomic CoCr V40 Femoral Heads.
- RECALL
Stryker is recalling rHead, uHead, Sigmoid Notch, Remotion, Radio Capitellum because packaging integrity (sterile barrier) of the packaging type KIT I may potentially be compromised by transportation.
- RECALL
A package labeled as Part #5901-S-4818, Lot MAC7C14, standard humeral head trial, contained part # 5901-E-4818 Lot MAC7C14, offset humeral head trial.
- RECALL
Stryker initiated a device recall of the Navigation System II-Cart, Camera Articulated Arm because there is a potential that the weld seam between the main stud and the two flaps on the Articulated Arm was not welded in the correct location, which may result in a potential failure of the arm joint.
- RECALL
Three customer complaints were received for the same batch of V40 LFIT Vitallium femoral heads (part number 6260-9-032, lot 48681201) alleging that the femoral head couldn't be assembled with its corresponding V40 stem trunnion.
- RECALL
Five customer complaints were received for the same batch of Trident PSL Shells (part number 540-11-50E lot 49073501) alleging that when the packages were opened there were no dome holes plugs present.
- RECALL
The Stryker NAV3i Platform Power Boxes produced between December 9, 2013 and March 7, 2014 may have been assembled without electrical insulation of the soldering joints
- RECALL
In certain operating room environments, a colored screen image occurs with the 1488 Cameras that were manufactured during a specific time period
- RECALL
Surgeons have experienced unthreading of the screwdrivers outer shafts during use.
- RECALL
Stryker has received a report that single size 3.5 stem was packaged as size 2.5 stem resulting in a possible product mix.
- RECALL
Two product complaints reported that the Glenoid Reamer Spanner (Lot F3W7017) would not properly connect to the Glenoid Spherical Reamer.
- RECALL
An incorrect laser mark was noted on specific lots of product, incorrectly implying a stem size of 9, when the product is actually size 8.
- RECALL
Stryker Orthopaedics has become aware that a size 3 Accolade stem was in a box labeled as a size 5 Accolade stem.
- RECALL
Recalled device was packaged with the incorrect angled blade. The labeling indicates a 12 degree angle but the product has a 40 degree angle.
- RECALL
The CuttingEdge Advantage Rasp Handle, Straight Rasp Handle, and Specialty Head Center Accolade Broach Handle may fracture in two pieces along the width of the body under the striking plate. This may extend surgical time under anesthesia, cause trauma to the surgeon or patient, or contaminate the surgical site.
- RECALL
Packaging mix up between the Taper V40 Femoral Head and the LFIT V40 Femoral Head.
- RECALL
Sterilization issue: During post-sterilization inspection of the outer blister packaging of the affected lots, it was determined that the outer blister did not meet the required minimum seal width.
- RECALL
Circlip component used to suspend flat panel and navigation arm system may become dislodged.
- RECALL
Fracture of Stem Neck - The firm recently performed laboratory testing indicates that there may be a potential increased risk of stem neck fractures when a V40 +16mm offset femoral head is mated with certain Accolade TMZF femoral stems in patients classified as overweight or obese.
- RECALL
Some components have disassociated post-operatively resulting in additional surgery to the patient.
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