
Breg · Model Polar Care Cube
Proven reliability and effectiveness. Strong pump for optimal durability. High flow rate results in even pad temperature. Provides motorized cold treatment for 6-8 hours Examples of Use. Post Operative. Arthroscopic Procedures. Reconstructive Procedures. Plastic Surgery. General Surgery. Post-Trauma. Chronic Pain. Physical Therapy.
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 silent or running with no water movement, pad not cooling.
Root cause: Air lock in the connector, ice too small or insufficient, kinked hose, clogged foam filter, low power, or the unit below the pad.
Symptoms: Flow drops over time, pad cools unevenly.
Root cause: Debris in the foam filter under the lid.
Symptoms: Pad does not fill with water when applied.
Root cause: Air lock, pad above the unit, or bandages/straps too tight over the pad.
Symptoms: Water around the unit or hose connection.
Root cause: Worn connector seal or lid seal.
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 |
|---|---|---|---|
| Circulation pump | Periodic replacement | $$ | Moderate |
| Foam filter and filter cap | Frequent wear item | $ | Easy |
| Therapy pad | Frequent wear item | $$ | Easy |
| Hose / connector seals | Periodic replacement | $ | Easy |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
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.
Synced live from the FDA openFDA API.
They may not have been sealed prior to sterilization. Products with unsealed pouches will be non-sterile.
The recall was initiated because Breg has determined that some Sterile Polar Pads products manufactured from January 2010 to October 2012 may have sustained damage to the product packaging which may compromise product sterility assurance.
This recall has been initiated due to confirmation that the Polar Dressing, Knee/MU/Shldr Intelli-Flo-Breg does not meet the required thickness as specified. The dressing in the sterile pouch measures a thickness of 0.010" instead of 0.020". This change in thickness makes the dressing thinner, less durable and subject to tearing. The product is mislabeled.
Power supplies short-circuited at the electrical outlet upon initial use of the power supply, causing the circuit breaker for the electrical outlet to trip.
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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