
Stryker · Model MX-Pro
Scientifically optimized lift bar design Positive action height adjustment One-hand release breakaway head section with safety bar Oversize wheels maximize mobility on all types of terrain Sealed fluid resistant bolster mattress One-four point shoulder harness restraint Two lap belt restraints One-hand release, fold down side rails One-hand release, infinite positioning, lift assist pneumatic backrest Fold-down side rails enable caregiver-patient access even in the smallest spaces. X-frame that features 7 height positions Floor-mount safety hook.
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: Pump will not raise the deck, or the deck settles under load.
Root cause: Worn hydraulic pump / seals, an internal valve leak, or low hydraulic fluid.
Symptoms: Brake will not hold, fifth-wheel steer ineffective, castor shimmy.
Root cause: Worn brake linkage, castors, or the fifth-wheel mechanism.
Symptoms: Backrest will not raise / hold, gas strut weak, pneumatic assist failed.
Root cause: Worn gas spring / strut or the release mechanism.
Symptoms: Siderails will not latch or drop, IV pole loose, litter attachments worn.
Root cause: Worn latches, detents, or accessory sockets.
Symptoms: Drive assist will not engage or is weak, drive-fault code.
Root cause: Drive battery, motor / controller, or the throttle.
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 |
|---|---|---|---|
| Hydraulic pump / seal kit | Major service part | $$ | Moderate |
| Castor / brake-linkage set | Periodic replacement | $$ | Moderate |
| Backrest gas spring / strut | Periodic replacement | $$ | Fairly easy |
| Siderail latch / accessory sockets | Major service part | $$ | Fairly easy |
| Drive battery (powered stretchers) | 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.
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.
Transport Cot has insufficient volume of epoxy to assemblies installed in the head section and foot sectioning system may result in separation of head end or foot end from the cot and result in unexpected disengagement while loading/unloading or transport.
Cot may experience unintended motion due to damaged cables. Potential risk of soft tissue injury to patients such as scrapes or bruises resulting from the cot lowering faster than expected.
Ambulance Cots may not meet crash test standard BS EN 1789
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.
Complaints of smoke coming from the foot end of the cot. This reportedly occurred when either the battery was placed into the cot or shortly after placing the battery into the cot. In addition to the alleged smoking, one of the reports had also noted that when the user attempted to lower the cot (prior to the alleged smoking) the device went into high speed retract and then a few moments later i
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.
Device will not able to assign the correct time/date stamp for saved filed after December 31, 2009. On Jan 1, 2010, the device system date for all SDC Pro 2 units will re-start from 1 Oct 2001 and begin incrementing from that point onwards. The system date will be incorrect and users will not be able to correct this issue. Problem will not affect how pictures or videos are captured using SDC Pro
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.
The head section wheel assembly may flex outward from the cot because the head section wheel bolts, which hold the assembly upright, may back out.
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.
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