Drager Resuscitaire Series

Skin Temperature Probe or Servo-Control Fault

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Asset Type

Infant Warmer

Manufacturer

Drager

Model

Resuscitaire Series

What This Guide Helps With

Troubleshooting missing, unstable, or inaccurate skin temperature readings and servo-mode operation affected by probe, connection, setup, or controller faults.

Step-by-Step Troubleshooting

1. Ensure Patient Safety First

If the warmer is supporting an infant, notify clinical staff immediately and move the patient to a known-working warmer or approved thermal-support method before troubleshooting.

Do not troubleshoot an unresolved skin temperature or servo-control fault while the warmer is relied upon for patient temperature regulation.

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

Why it matters: In Servo Mode, the Resuscitaire adjusts heater output based on the connected skin temperature probe. An unreliable probe signal can interfere with temperature regulation.

2. Confirm the Reported Fault and Operating Mode

Power on the warmer away from patient use and document the reported symptom:

Confirm whether the issue occurs in Servo Mode, since this mode depends on the skin temperature probe for automatic heater control.

Expected outcome: The complaint is reproduced and clearly identified as a probe-detection, temperature-reading, or servo-control problem.

3. Inspect the Skin Temperature Probe Externally

Inspect the probe and its cable for:

Do not use a visibly damaged probe for further clinical testing.

Expected outcome: The probe is either found intact for continued evaluation or identified as damaged and removed from use.

4. Verify the Probe Is Fully Connected

Disconnect and firmly reconnect the skin temperature probe at the designated temperature-probe connection. Ensure the connector is correctly oriented and fully seated.

Observe whether the probe alarm clears and whether a stable skin temperature value appears.

Expected outcome: A loose or partially seated connection is corrected, and a stable temperature reading is restored. If resolved, document the correction and stop troubleshooting.

Why it matters: The Resuscitaire identifies probe conditions including short circuit, open circuit, or no probe.

5. Inspect the Probe Port and Nearby Connections

Visually inspect the probe receptacle on the warmer for:

Do not insert tools into the connector or attempt internal repairs during this evaluation.

Expected outcome: The probe port appears clean and undamaged, or visible port damage supports removal from service for repair.

6. Test With a Known-Good Compatible Skin Temperature Probe

Using a clean, approved, known-good compatible skin temperature probe, connect it to the warmer and recheck the temperature display and Servo Mode behavior.

Expected outcome:

Why it matters: This separates a removable accessory failure from a likely device-level fault without internal disassembly.

7. Verify Displayed Temperature Is Reasonable and Stable

With the known-good probe connected during bench evaluation, verify that the displayed skin temperature is present, stable, and reasonable for the test condition.

The Resuscitaire skin temperature display range is specified as 18°C to 43°C, with accuracy specified as ±0.2°C from 31°C to 37°C.

Expected outcome: A stable, plausible displayed temperature supports proper probe detection. Missing, erratic, or clearly implausible readings indicate the unit should not be returned to service.

8. Check Servo Mode Response Without Patient Use

Place the warmer in Servo Mode only during controlled bench evaluation, using an approved connected probe and following departmental testing practice.

Observe whether:

The Resuscitaire Servo Mode uses a dual thermistor temperature probe and has a baby-temperature alarm condition of approximately ±1°C from the set point.

Expected outcome: Servo Mode recognizes the probe and operates without unresolved alarms. If normal function is restored after replacing the probe, complete required verification before returning the device to service.

9. Review Alarm Behavior and Final Device Status

Document any alarms or indications observed during testing, including:

Expected outcome: The device either passes evaluation with a confirmed accessory correction or remains faulted and requires repair evaluation.

If the Problem Persists

If the fault continues after confirming safe setup, reseating the connection, visually inspecting the port, and testing with a known-good compatible skin temperature probe, common external causes have been ruled out.

The issue is likely internal to the probe input circuit, temperature-monitoring function, servo-control system, or controller module.

The device should be:

Do not return the warmer to clinical use with an unresolved probe or servo-control fault. Knowing when to stop and escalate is proper troubleshooting.

Clinical Use Tip

Never troubleshoot a servo-control or skin temperature probe fault while an infant depends on the affected warmer for thermal support. Move the patient to safe alternate equipment first, then evaluate the warmer away from patient use.

Work Order Documentation (CCR Method)

CCR = Complaint, Cause, Resolution

Complaint

What was reported by the clinical staff.

Example:
"Labor and Delivery reported that the Drager Resuscitaire displayed a probe fault and would not regulate temperature properly in Servo Mode."

Cause

What was observed during troubleshooting.

Example:
"Skin temperature probe produced an intermittent reading, and the fault cleared when tested with a known-good compatible probe."

Resolution

What action was taken.

Example:
"Removed the defective skin temperature probe from use, replaced it with a functional probe, verified stable temperature display and Servo Mode operation, and returned the warmer to service."

Helpful Details to Include (If Known)

Final Thought

Skin temperature and servo-control faults must be handled conservatively because accurate thermal regulation is essential for neonatal safety. Rule out the probe and external connection first, verify operation only away from patient use, and escalate promptly when the warmer cannot be proven safe. Clear CCR documentation protects both patient care and future troubleshooting.

That is successful troubleshooting.

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