Stryker · Model MX-PRO R3
• Easy-to-use release handle design • High visibility powder-coated frame • Lightweight, rugged aluminum construction • Seven height positions • Integrated bumper system • Lift-capable safety bar • Perforated littersurface • One-hand release breakaway head section with safety bar • Shock positioning
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.
Symptoms: Won't hold position, rolls when locked.
Root cause: Brake pad wear or linkage failure.
Symptoms: Hard to push straight, wobbles or drags.
Root cause: Bearing wear or a flat-spotted wheel.
Symptoms: Visible crack or looseness at a joint.
Root cause: Repeated load cycling.
Symptoms: Torn or cracked cover, exposed padding.
Root cause: Cleaning-chemical and UV degradation, routine wear.
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.
Consumable - replace on visible wear or tear.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Upholstery / seat or surface cover Consumable - replace on visible wear or tear. | Periodic replacement | $ | Easy |
| Frame hardware (bolts, pins, bushings) | Major service part | $ | Fairly easy |
| Caster wheel assembly | Periodic replacement | $$ | Fairly easy |
| Brake / wheel-lock mechanism | Periodic replacement | $$ | 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 structured starting point derived from the failure modes above. 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.
Neurovascular devices did not meet the minimum sample size required for endotoxin testing during manufacturing processes and are out of compliance with the AAMI ST72 standard, so these devices may exceed the acceptable limits of endotoxin levels; high levels of endotoxins may increase the risk of fever, shock and aseptic meningitis.
The microcatheter IFU contains an intended use that has not been evaluated by the FDA.
Laser etching which indicates whether the device is in compression or distraction mode appears to be on the wrong side of the lever arm
Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs were manufactured using a carton sleeve where the pre-printed contents on the back of the sleeve did not match the physical contents of the pack.
The Foot Rest Kit may have the wrong pivot spacers making the joint more susceptible to relaxation and prone to fatigue. There is a moderate risk of injury to the patient should the handles become detached during use.
The front of the handle may become detached from the chair, which could result in a patient fall or an operator injury.
Handle could come off. The bolts may back out over time, resulting in a risk of dropping the patient and/or injury to transport personnel, a delay in medical treatment, or a delay in evacuation.
Locking pins may be installed backward, and cot may drop from highest to lowest position when the users are not prepared for the drop.
Describe a symptom or error code. Bio answers from this device's own documented error codes, failure modes, parts, and guides.
Ask Bio →