Getinge Servo-i

Edi / NAVA Module Not Recognized

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Asset Type

Ventilator

Manufacturer

Getinge

Model

Servo-i

What This Guide Helps With

Troubleshooting an Edi module that is missing, intermittently detected, or unavailable for Edi monitoring, NAVA, or NIV NAVA operation.

Step-by-Step Troubleshooting

1. Ensure Patient Safety First

Do not troubleshoot an Edi or NAVA recognition problem while the Servo-i is actively supporting a patient who depends on NAVA ventilation.

Expected outcome: The patient is safely supported without relying on unavailable or unreliable Edi functionality.

Continue Clinical Engineering troubleshooting only after the affected equipment can be evaluated safely.

2. Confirm the Exact Reported Condition

Determine whether:

Record the exact message and photograph the screen when permitted.

Expected outcome: The failure is identified as a module-recognition problem rather than an Edi catheter signal or positioning problem.

3. Confirm That the Servo-i Is Properly Configured for Edi/NAVA

Verify that the ventilator is a Servo-i configuration equipped and authorized for the required Edi monitoring and NAVA functions.

NAVA uses the patient’s Edi signal to control ventilatory assistance, and availability depends on the appropriate ventilator configuration, hardware, and enabled functionality.

Expected outcome: Edi/NAVA functionality is confirmed as installed and expected to be available.

If the option is not installed or activated, stop troubleshooting and refer the issue to the appropriate Getinge service or licensing process.

4. Power Down the Ventilator Safely

Shut down the Servo-i using the normal power-off procedure.

Expected outcome: The system is safely de-energized for an external connection inspection.

5. Inspect the Edi Module Externally

Remove the Edi module according to the facility’s approved handling procedure and inspect it for:

Do not open the module housing.

Expected outcome: The module is externally clean, dry, and free of obvious physical damage.

If damage, liquid intrusion, unusual heat, or burning odor is found, remove the module from service and stop.

6. Inspect the Ventilator Module Connection

Use adequate lighting to inspect the corresponding Servo-i module slot or connection point.

Check for:

Do not probe connector contacts with metal tools or apply unapproved cleaners.

Expected outcome: The connection area is clean, dry, unobstructed, and undamaged.

7. Reseat the Edi Module

Reinstall the module carefully and verify that it is:

Reconnect power and restart the ventilator.

Expected outcome: The Servo-i detects the module during startup and makes the applicable Edi functions available.

If recognition is restored, complete operational verification before returning the ventilator to service, then stop.

8. Disconnect External Edi Accessories

If the module remains unrecognized, disconnect the Edi catheter cable and other external accessories from the module.

Restart or recheck the system with only the module installed.

This separates a module-recognition problem from an accessory cable, connector, or catheter-related issue.

Expected outcome: The module is recognized without the patient cable or catheter connected.

If recognition returns, inspect the disconnected cable and accessory connectors for contamination, bent contacts, strain damage, or incompatibility. Replace the suspect accessory with an approved known-good component.

9. Check the Edi Patient Cable and Connector

Inspect the Edi cable for:

Do not perform aggressive bending or twisting tests.

Expected outcome: The cable is intact and connects securely without causing module detection to drop.

A catheter-positioning or weak-Edi-signal problem should be handled separately after the ventilator consistently recognizes the Edi module.

10. Test With a Known-Good Compatible Edi Module

When facility policy and equipment availability permit, install a verified compatible Edi module from a functioning Servo-i.

Do not exchange modules between patients without completing required cleaning, disinfection, and infection-control procedures.

Expected outcome: The fault is isolated to either the original Edi module or the ventilator.

If the known-good module resolves the issue, stop and route the original module for repair.

11. Test the Suspect Module on a Known-Good Servo-i

When authorized, install the suspect Edi module on another compatible, non-clinical Servo-i test system.

Expected outcome: The module or ventilator is identified as the probable source of the failure.

12. Review Software and Configuration History

Determine whether the issue began after:

Compare the installed software and option configuration with facility records.

Do not attempt unauthorized software installation, option activation, or configuration changes.

Expected outcome: The ventilator’s configuration remains appropriate for its installed Edi/NAVA hardware.

13. Run the Approved Pre-Use Check

After reseating or substituting components, run the complete Servo-i pre-use check using the approved test circuit and gas supplies.

Confirm that:

Expected outcome: The ventilator and recognized Edi module complete operational verification without recurring faults.

Do not return the system to clinical use based only on the module appearing on the screen.

If the Problem Persists

If the Edi module remains unrecognized after configuration, seating, connectors, cables, accessories, and known-good substitution have been checked, common external causes have been ruled out.

The failure may involve:

The ventilator or affected module should be:

Do not open the Edi module or continue into internal board-level troubleshooting without the proper service documentation, training, test equipment, and authorization.

Knowing when to stop and escalate is proper troubleshooting.

Clinical Use Tip

Never troubleshoot Edi recognition, catheter connectivity, or NAVA availability while a patient depends on that function. Move the patient to verified support before manipulating modules, cables, or ventilator configuration.

Work Order Documentation (CCR Method)

CCR = Complaint, Cause, Resolution

Complaint

What was reported by the clinical staff.

Example:
"Respiratory therapy reported that the Servo-i did not recognize the installed Edi module and NAVA was unavailable."

Cause

What was observed during troubleshooting.

Example:
"The Edi module was not detected after reseating and cable removal but a known-good module was recognized, isolating the failure to the original module."

Resolution

What action was taken.

Example:
"Removed the defective Edi module from service, installed a verified replacement, completed the Servo-i pre-use check, and confirmed stable Edi module recognition."

Helpful Details to Include (If Known)

Final Thought

Patient safety comes first when Edi monitoring or NAVA becomes unavailable. Logical substitution testing can separate an accessory, module, configuration, or ventilator fault without unnecessary disassembly. Clear CCR documentation supports safe repair decisions and prevents defective components from returning to service.

That is successful troubleshooting.

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