Smiths Medical · Model Sims Level 1 System 1000
Sims Level 1 System 1000 Medical Blood Fluid Warmer.
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: No heat, or overheat alarm.
Root cause: Heater element or thermal cutoff failure.
Symptoms: Delivered fluid temperature out of set range.
Root cause: Inline/probe sensor aging or miscalibration.
Symptoms: False or missed air-in-line alerts.
Root cause: Air detector sensor drift or dirty optics.
Symptoms: Fluid leak, or won't prime.
Root cause: Worn cassette/tubing seat or cracked fitting.
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.
Single-use consumable.
Consumable in some designs.
Safety-critical; verify at PM.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Disposable tubing / cassette set Single-use consumable. | Consumable | $ | Easy |
| Heating element / plate | Periodic replacement | $$$ | Moderate |
| Temperature sensor / probe Consumable in some designs. | Periodic replacement | $$ | Fairly easy |
| Air-in-line sensor Safety-critical; verify at PM. | 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 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.
IV Fluid Administration Set may have a blockage of the recirculating warming fluid channel within the disposable administration set, causing an alarm condition of over-temperature during priming.
Inaccurate infusion rate-administration sets which are used with selected infusion pumps may have a defect which does not allow the pump valve to close completely.
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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