GE Healthcare B105 / B125 / B155 Series

CO2 Module Not Recognized or No Capnogram

On this page

Asset Type

Patient Monitor

Manufacturer

GE Healthcare

Model

B105 / B125 / B155 Series

What This Guide Helps With

Troubleshoots unavailable CO2 monitoring, module recognition, sampling accessories, blocked or wet sample paths, loose connections, and missing capnograms.

Step-by-Step Troubleshooting

1. Protect the Patient and Maintain Ventilation Monitoring

If capnography is clinically required and unavailable, provide another verified method of ventilation monitoring before troubleshooting.

Do not troubleshoot an unreliable CO2 channel while a patient depends on it.

Expected outcome: Required patient ventilation monitoring continues using reliable equipment.

2. Confirm the Exact CO2 Complaint

Determine whether:

Expected outcome: The problem is separated into module recognition, sampling-path, or signal-acquisition categories.

3. Inspect and Reseat External CO2 Connections

Inspect accessible CO2 module and cable connections for:

Reseat connections according to normal approved operating arrangements.

Expected outcome: The CO2 hardware is securely connected and recognized.

If reseating restores the parameter and normal capnogram, proceed to final verification.

4. Inspect the Sampling Accessories

For sidestream configurations, inspect the external sample line, airway adapter, water-management components, and other disposable sampling accessories as applicable.

Check for:

Do not attempt to clear single-use tubing with unapproved methods.

Expected outcome: The external sampling path is dry, open, correctly assembled, and securely connected.

If replacing an obstructed or wet disposable accessory restores the capnogram, proceed to final verification.

5. Confirm Compatible Accessories

Verify that CO2 sampling accessories or sensor components are approved for the installed CO2 monitoring configuration.

Do not assume that visually similar sampling accessories are interchangeable.

Expected outcome: Compatible CO2 accessories are installed.

6. Allow Appropriate Initialization

After reconnecting an appropriate CO2 module or sampling system, allow the parameter to initialize normally.

Observe whether status indicators progress to a usable monitoring condition without repeated disconnection.

Expected outcome: The CO2 parameter becomes available and remains recognized.

If recognition is restored and stable, continue with signal verification.

7. Substitute Known-Good External Components

When available, substitute compatible known-good components such as:

Change one item at a time.

Expected outcome: The problem follows a specific replaceable accessory or module, or remains with the monitor.

If a replaceable external item is confirmed faulty, replace it and continue to final verification.

8. Test With Approved CO2 Test Equipment

Off-patient, use approved test equipment or a controlled test method appropriate for the CO2 configuration.

Verify:

Do not attempt unauthorized calibration or adjustment.

Expected outcome: The monitor produces a stable CO2 waveform and value from a controlled input.

9. Inspect the Accessible Monitor Interface

Inspect the accessible module bay, input connector, or cable interface involved with CO2 monitoring for physical damage, contamination, or looseness.

Do not disassemble the monitor or module to repair internal connectors.

Expected outcome: The monitor-side interface appears intact and mechanically secure.

10. Perform Final Functional Verification

After correction, verify:

Expected outcome: CO2 monitoring is stable and suitable for return to clinical service.

If all checks pass, document and return the monitor to service.

11. Escalate Persistent CO2 Failure

If compatible known-good accessories and approved testing do not restore module recognition or capnogram acquisition, stop external troubleshooting.

Expected outcome: The affected monitor or module is removed from service for qualified evaluation.

If the Problem Persists

Sampling accessories, module seating, external interfaces, compatibility, and known-good test inputs have been evaluated. Remaining possibilities may include internal module failure, monitor-module communication, sampling pump or sensing components, configuration, or another service-level condition.

The affected equipment should be:

After repair, verify parameter recognition, capnogram acquisition, numeric response, alarms, and required overall monitor functions.

Knowing when the external CO2 path has been ruled out and service-level evaluation is required is proper troubleshooting.

Clinical Use Tip

A numeric EtCO2 value without a dependable capnogram should not be treated as complete verification of the capnography channel.

Work Order Documentation (CCR Method)

CCR = Complaint, Cause, Resolution

Complaint

What was reported by the clinical staff.

Example:
"Respiratory staff reported that the B125 monitor showed no capnogram despite the CO2 parameter being available."

Cause

What was observed during troubleshooting.

Example:
"Clinical Engineering found the external CO2 sample line was occluded and confirmed normal operation with a known-good sampling line."

Resolution

What action was taken.

Example:
"Replaced the occluded sample line, verified a stable capnogram and CO2 value with approved testing, confirmed alarm operation, and returned the monitor to service."

Helpful Details to Include (If Known)

Final Thought

Maintain required ventilation monitoring, inspect the entire external CO2 sampling and connection path before assuming internal failure, and use compatible known-good components to isolate the cause. Escalate persistent module or acquisition failures and clearly document verification.

That is successful troubleshooting.

Related Guides

Was this guide helpful?

Don't see a guide you need?

Suggest a Guide