Drager Resuscitaire Series

Alarm, Display, or Power Fault

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Asset Type

Infant Warmer

Manufacturer

Drager

Model

Resuscitaire Series

What This Guide Helps With

Troubleshooting loss of power, abnormal display operation, Power Fail/System Fail alarms, or alarm conditions caused by external connections or setup issues.

Step-by-Step Troubleshooting

1. Ensure Patient Safety First

If the Resuscitaire is supporting an infant, notify clinical staff and move the infant to another approved warming/resuscitation device before troubleshooting.

Do not continue using the warmer when power, display, or alarm operation is unreliable.

Expected outcome: The infant is safely supported by alternate equipment before the affected warmer is evaluated.

Why it matters: The Resuscitaire provides warming support and may include resuscitation components used during neonatal stabilization. A power, display, or alarm fault can prevent dependable monitoring or warming operation.

2. Confirm the Reported Fault

Power on the unit, if safe to do so, and observe the control panel for:

Document whether the fault is constant, intermittent, or occurs only during startup or warming operation.

Expected outcome: The actual alarm, display, or power symptom is identified before parts or accessories are suspected.

If the reported condition cannot be reproduced: Perform normal operational verification according to department procedure before returning the device to service.

3. Inspect for Obvious Damage or Unsafe Conditions

Disconnect the unit from patient use and inspect the warmer externally for:

Expected outcome: No external damage or hazardous condition is found.

If damage, liquid intrusion, burning odor, or excessive heat is present: Stop troubleshooting, remove the device from service, and send it for repair evaluation.

4. Verify the AC Power Source

Confirm the warmer is connected directly to an approved hospital-grade outlet. Test the outlet with an appropriate outlet tester or a known-working clinical device in accordance with facility practice.

Do not rely only on the room’s wall indicator or assume the outlet is functional.

Expected outcome: The outlet provides reliable AC power.

If the outlet is defective or switched off: Move the warmer to a verified outlet and retest. If normal operation returns, document the external power-source issue and stop.

Why it matters: The Resuscitaire identifies interrupted AC power as a Power Fail condition.

5. Inspect the Power Cord and Connection

Verify that the power cord is fully seated, secured where applicable, and free from cuts, exposed conductors, loose blades, bent pins, or evidence of strain.

Gently check whether movement of the cord or plug causes the display or power indication to flicker.

Expected outcome: The unit remains powered consistently without intermittent operation.

If a removable cord is damaged or suspect: Replace it with an approved known-good cord and retest.

If power or display operation still cuts out with a verified outlet and known-good cord: Remove the device from service for bench evaluation.

6. Check the Power Switch and Startup Behavior

With the warmer connected to verified AC power, turn the unit on and observe whether:

Expected outcome: The controller powers on and remains stable without an unresolved fault indication.

If the unit does not power on, repeatedly resets, has a blank or unreadable display, or indicates System Fail: Do not continue clinical use. Remove it from service for repair evaluation.

7. Differentiate a Power Fault From a Clinical Alarm Condition

If the display is operating but an alarm is active, identify the alarm category before assuming the controller has failed. The Resuscitaire controller may indicate:

Expected outcome: A correctable accessory or operating-condition alarm is distinguished from a power or internal system fault.

If a System Fail indication is present: Stop and escalate; do not attempt to clear it through repeated operation.

8. Check the Skin Temperature Probe and Connector, When Applicable

If the alarm is related to Probe, Baby Temperature, or unexpected skin temperature display behavior:

Expected outcome: A functional probe is recognized and temperature-related alarm behavior resolves when the accessory was the cause.

If replacing or reseating the probe resolves the issue: Verify normal operation and document the defective or loose probe as the cause, then stop.

If the fault remains with a known-good probe: Remove the warmer from service for further evaluation.

9. Check Whether the Alarm Is Related to Manual Mode Operation

If staff report repeated alarm activation while the warmer otherwise powers and displays normally, confirm whether the unit was operating in Manual Mode.

The Resuscitaire includes a Check Patient alarm function during Manual Mode operation; this may be reported as a device alarm even when the display and power system are operating normally.

Expected outcome: The reported alarm is correctly identified as either expected mode-related behavior or an unresolved abnormal condition.

If expected alarm behavior is confirmed: Educate the reporting department as appropriate, document the finding, and complete operational verification before return to service.

10. Evaluate Display Reliability During Basic External Testing

Observe the display while performing safe, non-patient testing:

Expected outcome: The display remains stable and provides reliable information.

If the display is blank, incomplete, frozen, flickering, or unreliable after power and accessory checks: Remove the unit from service. A warmer with an unreliable display cannot be trusted for clinical use.

11. Perform Final Operational Verification

After resolving an external issue such as outlet failure, damaged cord, loose connection, or defective probe, complete the department-approved operational and safety verification before returning the warmer to use.

Confirm:

Expected outcome: The warmer operates normally and passes required verification.

If any alarm, display, or power concern remains unresolved: Do not return the unit to service.

If the Problem Persists

If the Resuscitaire continues to have a blank or unreliable display, unexplained alarm behavior, System Fail indication, repeated power interruption, or inability to operate normally after external checks, common external causes have been ruled out and the fault is likely internal.

The device should be:

Knowing when to stop is proper troubleshooting. Do not continue attempting to operate an infant warmer with unresolved alarm, display, or power reliability concerns.

Clinical Use Tip

Do not troubleshoot an infant warmer while it is actively supporting an infant. Move the infant to another approved warming/resuscitation device first, then evaluate the affected warmer only when it is safe to do so.

Work Order Documentation (CCR Method)

CCR = Complaint, Cause, Resolution

Complaint

What was reported by the clinical staff.

Example:
"Clinical staff reported that the Drager Resuscitaire displayed a Power Fail alarm and intermittently lost the control panel display during setup."

Cause

What was observed during troubleshooting.

Example:
"Found the warmer connected to a faulty AC receptacle that did not provide stable power; the warmer operated normally when connected to a verified outlet."

Resolution

What action was taken.

Example:
"Removed the original outlet from use through the appropriate facilities process, verified stable warmer power and display operation from a known-good outlet, completed operational checks, and returned the device to service."

Helpful Details to Include (If Known)

Final Thought

An infant warmer with unreliable power, alarm operation, or display function must be approached cautiously. Start with patient safety, rule out simple external causes logically, and escalate promptly when reliable operation cannot be confirmed. Clear CCR documentation preserves the troubleshooting path and supports safe equipment decisions.

That is successful troubleshooting.

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