Cincinnati Sub-Zero · Model Gelli-Roll Blanket
Reduces set-up and breakdown time Easy to clean with disinfectants Allows complete access to the patient Supports most patients, infant to bariatric Self-sealing hose connections Can be used for warming or cooling the patient
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, overheat alarm.
Root cause: Element or thermal fuse failure.
Symptoms: Setpoint error, alarm.
Root cause: Sensor aging.
Symptoms: Uneven warming, hotspot.
Root cause: Blower 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.
Common R&R.
Consumable per patient.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Heating element / thermal fuse Common R&R. | Periodic replacement | $$$ | Moderate |
| Blower fan | Periodic replacement | $$ | Fairly easy |
| Temperature probe Consumable per patient. | 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.
No documents available for this device yet.
Synced live from the FDA openFDA API.
Evidence supports that when customers performed a fuse replacement as part of a March 2017 field action, the fuse clips became stretched and were no longer mechanically tight with the fuse, creating a host spot that led to discoloration on the board due to overheating and shut down of the device.
Potential for membrane (control panel) switch errors leading to an inability of the device to change control settings or an unintended change to control settings.
Reports that the Rectal/ Esophageal Temperature Probes are not reading correctly. This situation causes the Blanketrol device, which the probes connect to, to shut down operation and display a 'check probe' error.
Due to its design the circuit breaker on the device could trip causing it to shut down and not provide heated air to the blanket.
A component defect. The recalling firm determined that one of the connectors attached to the firm's WarmAir 134 device's Printed Circuit Board (PCB) can overheat. Should this event occur, the excess heat build up within the device may result in damage to the device's external case and/or melting of some of the internal components of the unit.
Product is labeled as "Sterile". It was observed that incomplete seals were created in the packaging materials during production. When the seal is compromised, the sterility of the product inside the package cannot be assured.
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