Arjo · Model Sara Stedy
Innovative pivoting seat improves transfer efficiency and patient stability Easy to open chassis Total-lock castors Built in seat handgrips Better knee support Lower chassis
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: Short runtime, low-battery alarm.
Root cause: Aged battery.
Symptoms: Intermittent signal/power.
Root cause: Repeated flexing.
Symptoms: Loose device, vibration damage.
Root cause: Docking latch 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.
Critical for transport; spares mandatory.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Rechargeable battery pack Critical for transport; spares mandatory. | Frequent wear item | $$$ | Fairly easy |
| Docking cradle / latch | Periodic replacement | $$ | Fairly easy |
| Patient cable set | Periodic replacement | $$ | Easy |
Relative cost: $ lowest · $$$$ 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.
ArjoHuntleigh has received a limited number of customer reports concerning injuries related to an exposed metal support bracket when the proactive knee pad assembly is removed.
There is the potential for the slings to come apart, potentially allowing injury to the patient.
The sling ropes were manufactured with insufficient rope length past the knot to prevent the knot from coming loose.
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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