GE Healthcare Avance

Flow Sensor Calibration Failure

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Asset Type

Anesthesia Machine

Manufacturer

GE Healthcare

Model

Avance

What This Guide Helps With

Troubleshooting failed flow-sensor calibration caused by improper removal, moisture, contamination, incorrect installation, damaged sensors, or breathing-system connection problems.

Step-by-Step Troubleshooting

1. Ensure Patient Safety First

Do not calibrate, remove, or exchange flow sensors while the Avance is supporting an active patient.

If the failure occurs during clinical use:

Expected outcome: Patient care no longer depends on equipment with questionable flow or volume measurement.

2. Confirm the Exact Failure

Record the complete displayed message and determine whether the failure involves:

Expected outcome: The affected sensor and failure behavior are clearly identified.

3. Verify the Machine Is in the Correct State

Place the Avance in Standby and ensure that no patient is connected.

Access the flow-sensor calibration through the applicable calibration menu for the installed software version. Follow the on-screen instructions exactly.

GE guidance specifies that the sensors are removed from the breathing system during routine flow calibration.

Expected outcome: The system accepts the calibration request and displays the required preparation steps.

4. Remove Both Flow Sensors as Directed

Remove the inspiratory and expiratory flow sensors from their installed positions before starting calibration.

Confirm that:

Expected outcome: The machine recognizes the zero-flow condition required for calibration.

If calibration completes successfully, reinstall the sensors correctly, perform the required checkout, and stop troubleshooting.

5. Inspect for Moisture or Condensation

Examine both sensors for:

Allow the sensors to dry completely according to facility and manufacturer-approved handling procedures. Do not use unapproved heat, compressed air, or objects inside the sensing passages.

Expected outcome: Both sensors are clean and completely dry before another calibration attempt.

6. Inspect for Contamination or Physical Damage

Visually inspect each sensor for:

Do not scrape or probe the sensing elements.

Expected outcome: Only clean, undamaged sensors remain in use.

Remove any visibly damaged sensor from service.

7. Check Sensor Identification and Placement

Confirm that the inspiratory and expiratory sensors are installed in their correct locations and orientations.

Check that:

Expected outcome: Both sensors are correctly positioned and recognized by the system.

8. Reseat the Breathing-System Connections

Inspect and reseat the accessible breathing-system assembly around the flow sensors.

Look for:

Expected outcome: The breathing system is completely and correctly assembled without stressing the sensors.

9. Repeat the Flow-Sensor Calibration

Remove the sensors again when instructed and repeat the calibration.

Do not move the machine, disturb the sensor ports, or create airflow near the open sensor locations while calibration is running.

Expected outcome: Calibration completes without an error message.

If successful:

10. Test With Known-Good Sensors

When permitted by facility policy, install a compatible, known-good pair of GE-approved flow sensors and repeat calibration.

GE describes these sensors as critical to accurate airway-flow and ventilation measurement.

If calibration succeeds, the original sensor or sensor pair is defective or out of specification.

If calibration still fails, the problem may involve the sensor interface, wiring, breathing-system electronics, or internal measurement circuitry.

Expected outcome: The test distinguishes a sensor problem from a machine-side fault.

11. Perform a Complete Checkout

After any sensor replacement, reseating, or successful calibration, complete the manufacturer-required pre-use checkout.

Verify:

Expected outcome: The machine passes all required functional and safety checks before clinical use.

If the Problem Persists

If calibration continues to fail after both sensors have been removed correctly, dried, inspected, reseated, and exchanged with known-good sensors, common external causes have been ruled out.

The failure may involve the sensor connector assembly, internal wiring, signal-processing electronics, or another internal breathing-system component.

The device should be:

Knowing when to stop and escalate is proper troubleshooting. GE restricts detailed life-support equipment service information to appropriately trained personnel.

Clinical Use Tip

Never troubleshoot questionable flow or volume measurements on an active patient. Transfer care first, then evaluate the machine with approved test equipment in a controlled setting.

Work Order Documentation (CCR Method)

CCR = Complaint, Cause, Resolution

Complaint

What was reported by the clinical staff.

Example:
"Anesthesia staff reported that the GE Avance displayed a flow-sensor calibration failure and would not provide reliable volume measurements."

Cause

What was observed during troubleshooting.

Example:
"The expiratory flow sensor contained visible condensation and failed calibration until it was dried and correctly reseated."

Resolution

What action was taken.

Example:
"Dried and reinstalled both flow sensors, completed flow calibration and machine checkout, verified stable volumes with a test lung, and returned the Avance to service."

Helpful Details to Include (If Known)

Final Thought

Flow-sensor calibration failures should be approached by protecting the patient, confirming correct calibration conditions, checking moisture and installation, and testing known-good sensors before suspecting an internal fault. Clear CCR documentation preserves the findings and supports safe escalation.

That is successful troubleshooting.

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