
Stryker · Model Manual
Best-In-Class Low Height. Retractable Fifth Wheel. Centrally-Located Brake. Removable Crank Handles. Siderail Positioning. CPR Release.
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: Backrest, knee, height, Trendelenburg or the boost / turn assist will not move from the siderail or caregiver controls.
Root cause: Failed linear actuator, a control-board fault, a control-panel fault, or a pinched / damaged control cable.
Symptoms: Bed will not brake or release, drifts, central brake pedal ineffective.
Root cause: Worn central-brake linkage or castor.
Symptoms: Weight reads implausibly or will not zero, bed-exit alarm false-triggers or fails.
Root cause: Load-cell drift or damage, or a scale-control fault.
Symptoms: Functions and alarms do not work during a power interruption, battery-fault indicator.
Root cause: Aged back-up battery or a charger fault.
Symptoms: Siderail will not latch, rattles, or the CPR release is slow / stiff.
Root cause: Worn siderail latch or the CPR mechanism.
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.
Recalibrate the scale after replacement.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Linear actuator (backrest / knee / height) | Major service part | $$$ | Difficult |
| Central-brake / castor assembly | Major service part | $$ | Difficult |
| Load cell / scale sensor set Recalibrate the scale after replacement. | Major service part | $$$ | Difficult |
| Back-up battery | Periodic replacement | $$ | Fairly easy |
| Siderail control panel / control board | Major service part | $$$ | Moderate |
Relative cost: $ lowest · $$$$ 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.
Synced live from the FDA openFDA API.
Stryker Neurovascular is recalling their DAC- Distal Access Catheter -038 136cm, a Distal Access Catheter by removal. The reason for the recall is: the DAC Lot #0000486382 was released with out-of-specification endotoxin results.
Potential for current software to miscount when scanning in multiple sponge-products from the same unique sponge-pack type
Malfunctioning of the Exeter Rasp/trial introducer/extractor Handle.
The Inserter Inner Shaft would not fit through the Inserter. The inner diameter of the cannulated shaft of the inserter was undersized.
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.
Surgeons have experienced unthreading of the screwdrivers outer shafts during use.
Stryker received four reports regarding a handle which separates at the point where it is welded to the shaft on the Xia 3 Anti-Torque Key during surgery.
Stryker Orthopaedics has become ware that there is the potential for the above referenced instruments to fracture in two pieces along the width of the body under the striking plate.
During testing and review, Stryker Endoscopy discovered that the sterilization parameters for the 132 degree C gravity steam sterilization cycle in the IFU may not consistently sterilize all instruments in the 45cm Laparoscopic Instruments Tray.
The Inner Shaft does not extend far enough from the tip of the Revision Screwdriver to fully engage the bone screw.
Sharp edges will cause a glove to tear and cut someone. Sharp edges on the slots machines in select lots of the Triathlon TS Femoral Trials, sizes 1-8, have been discovered.
The threaded part of the instrument may break when connected to the screw and potentially result in an adverse health consequence.
Insertion/Removal Difficulties: The Baseplate Impactor/Extractor may not assemble/disassemble easily to the baseplate.
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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