
Stryker · Model TPS
Total Performance Arthroscopy Shaver Console Works with the Stryker 12K Shaver Handpiece.
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.
Symptoms: Pressure droops or overshoots, poor distension, pressure or flow alarm.
Root cause: Pump-head / roller wear, a pressure-sensor fault, a leak in the tubing / inflow-outflow, or a blocked cannula.
Symptoms: Cassette / tubing not recognised, will not prime, leaks at the pump head.
Root cause: Cassette-detection switch or worn pump-head seals.
Symptoms: Poor outflow, cannot clear debris, outflow alarm.
Root cause: Outflow pump / valve or a blocked suction line.
Symptoms: Blade will not oscillate / rotate, weak cut, handpiece not recognised, footswitch dead.
Root cause: Worn shaver handpiece / motor, or its cable / footswitch.
Symptoms: Unresponsive touchscreen or keys, will not power on.
Root cause: Display / control board or power supply.
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.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Pump-head rollers / seals | Periodic replacement | $$ | Moderate |
| Pressure sensor / transducer | Major service part | $$ | Moderate |
| Cassette-detection switch | Periodic replacement | $$ | Moderate |
| Shaver handpiece / motor (shaver systems) | Periodic replacement | $$$ | Moderate |
| Footswitch | Periodic replacement | $$ | Fairly easy |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
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.
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.
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
No documents available for this device yet.
Synced live from the FDA openFDA API.
It was discovered that the silicone potting failed to properly cure after undergoing the prescribed curing possess. The potting material is used to insulate, stabilize and provide a moisture barrier to the TPS MicroDriver main Printed Circuit Board Assembly (PCBA). Inadequate cure of the silicone potting could potentially allow it to leak to the outside of the handpiece or cause an electrical ma
The safety margin values detailed in the Engineering Design were entered incorrectly into the programming software. Handpieces that have been programmed with the incorrect parameters could result in unintended activation. There is a potential for injury to the patient or user as a result of unintended forward or reverse activation. There is also the potential that the handpiece may not reach 100
There is a potential for these blades to break where the blade is welded on to the arbor. This hazard can result in the following harms: tissue damage due to the broken blade being aspirated or swallowed, additional surgery to remove a broken blade, infection due to an unretrieved device component, complications associated with increased time under anesthesia to retrieve a broken blade, osteomyeli
Product was packaged with an incorrect packaging material and therefore has a potential to be non-sterile which, if contaminated, could lead to a patient infection.
Lack of assurance of sterility.
Describe a symptom or error code. Bio answers from this device's own documented error codes, failure modes, parts, and guides.
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