Temperature ProbeRecalls & reported problems across all models
Fisher & Paykel Healthcare Limited · 3 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 32
- Deaths reported
- 1
- Injuries reported
- 1
- Recalls
- 0
We found 3 models of Temperature Probe by Fisher & Paykel Healthcare Limited in the FDA's device registry (GUDID). Together they are named in 32 adverse event reports in the FDA's MAUDE database, received between Apr 23, 2021 and Jan 19, 2026 — classified as 1 death, 1 injury, 30 malfunctions.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (27 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported Temperature Probe problems
Device problems
- Device Dislodged or Dislocated27
- Connection Problem2
- Loose or Intermittent Connection2
- Mechanical Problem1
- Moisture or Humidity Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions30
- Low Oxygen Saturation1
- Obstruction/Occlusion1
- Pneumonia1
- Respiratory Failure1
- Stroke/CVA1
Temperature Probe models
3 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Temperature Probe 900MR869Humidifier, Respiratory Gas, (Direct Patient Interface)1 death29 reports
- Temperature Probe 900MR868Humidifier, Respiratory Gas, (Direct Patient Interface)2 reports
- Temperature Probe 900MR861Humidifier, Respiratory Gas, (Direct Patient Interface)1 report
Recent Temperature Probe adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionJan 19, 2026Device Dislodged or Dislocated
A DISTRIBUTOR REPORTED ON BEHALF OF A HEALTHCARE FACILITY IN JAPAN, VIA A FISHER & PAYKEL (F&P) HEALTHCARE FIELD REPRESENTATIVE, THAT A 900MR869 TEMPERATURE/FLOW PROBE WAS IDENTIFIED TO BE EASILY DISLODGED FROM A TEMPERATURE PROBE PORT OF AN RT266 INFANT DUAL-HEATED EVAQUA2 BREATHING CIRCUIT DURING SETUP AND PRIOR TO PATIENT USE. THERE WAS NO REPORTED PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24110467 ↗MalfunctionDec 8, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
A DISTRIBUTOR REPORTED ON BEHALF OF A HEALTHCARE FACILITY IN JAPAN, VIA A FISHER & PAYKEL (F&P) HEALTHCARE FIELD REPRESENTATIVE, THAT A 900MR869 TEMPERATURE/FLOW PROBE WAS IDENTIFIED TO BE EASILY DISLODGED FROM A TEMPERATURE PROBE PORT OF AN RT265 INFANT DUAL-HEATED EVAQUA2 BREATHING CIRCUIT DURING SETUP AND PRIOR TO PATIENT USE. THERE WAS NO REPORTED PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23752231 ↗MalfunctionDec 2, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
A HEALTHCARE FACILITY IN COLORADO REPORTED VIA A FISHER & PAYKEL (F&P) HEALTHCARE FIELD REPRESENTATIVE THAT 97 900MR869 TEMPERATURE/FLOW PROBES WERE FOUND DISLODGING FROM AN RT266 INFANT DUAL-HEATED EVAQUA2 BREATHING CIRCUIT DURING SET-UP AND PRIOR TO PATIENT USE. THERE WAS NO REPORTED PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23701163 ↗MalfunctionNov 30, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
A DISTRIBUTOR REPORTED ON BEHALF OF A HEALTHCARE FACILITY IN JAPAN, VIA A FISHER & PAYKEL (F&P) HEALTHCARE FIELD REPRESENTATIVE, THAT TWO 900MR869 TEMPERATURE/FLOW PROBES WERE IDENTIFIED TO BE EASILY DISLODGED FROM A TEMPERATURE PROBE PORT OF AN RT265 INFANT DUAL-HEATED EVAQUA2 BREATHING CIRCUIT DURING SETUP AND PRIOR TO PATIENT USE. THERE WAS NO REPORTED PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23677413 ↗MalfunctionNov 17, 2025Connection Problem; Device Dislodged or Dislocated; Connection Problem; Device Dislodged or Dislocated
A DISTRIBUTOR REPORTED ON BEHALF OF A HEALTHCARE FACILITY IN JAPAN, VIA A FISHER & PAYKEL (F&P) HEALTHCARE FIELD REPRESENTATIVE, THAT THE TEMPERATURE/FLOW PROBE DISLODGED FROM A TEMPERATURE PROBE PORT OF AN RT265 INFANT EVAQUA2 BREATHING CIRCUITS DURING SET UP AND PRIOR TO PATIENT USE. THERE WAS NO REPORTED PATIENT CONSEQUENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23577923 ↗MalfunctionOct 9, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
A DISTRIBUTOR REPORTED ON BEHALF OF A HEALTHCARE FACILITY IN JAPAN, VIA A FISHER & PAYKEL (F&P) HEALTHCARE FIELD REPRESENTATIVE, THAT SIX 900MR869 TEMPERATURE/FLOW PROBES WERE IDENTIFIED TO BE EASILY DISLODGED FROM A TEMPERATURE PROBE PORT OF AN RT265 INFANT DUAL-HEATED EVAQUA2 BREATHING CIRCUIT DURING SETUP AND PRIOR TO PATIENT USE. THERE WAS NO REPORTED PATIENT CONSEQUENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23262844 ↗MalfunctionSep 24, 2025Loose or Intermittent Connection; Loose or Intermittent Connection
A HEALTHCARE FACILITY IN CANADA REPORTED VIA A FISHER & PAYKEL (F&P) HEALTHCARE REPRESENTATIVE THAT A 900MR869 TEMPERATURE/FLOW PROBE WAS IDENTIFIED TO BE LOOSE AT THE PATIENT-END TEMPERATURE PROBE PORT OF AN RT132 INFANT BREATHING CIRCUIT DURING SETUP AND PRIOR TO PATIENT USE. THERE WAS NO REPORTED PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23140175 ↗MalfunctionSep 18, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
A DISTRIBUTOR REPORTED ON BEHALF OF A HEALTHCARE FACILITY IN JAPAN, VIA A FISHER & PAYKEL (F&P) HEALTHCARE FIELD REPRESENTATIVE, THAT A 900MR869 TEMPERATURE/FLOW PROBE WAS IDENTIFIED TO BE EASILY DISLODGED FROM THE PATIENT-END TEMPERATURE PROBE PORT OF AN RT265 INFANT DUAL-HEATED EVAQUA2 BREATHING CIRCUIT DURING SETUP AND PRIOR TO PATIENT USE. THERE WAS NO REPORTED PATIENT CONSEQUENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23092700 ↗MalfunctionSep 18, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
A DISTRIBUTOR REPORTED ON BEHALF OF A HEALTHCARE FACILITY IN JAPAN, VIA A FISHER & PAYKEL (F&P) HEALTHCARE FIELD REPRESENTATIVE, THAT A 900MR869 TEMPERATURE/FLOW PROBE WAS IDENTIFIED TO BE EASILY DISLODGED FROM THE PATIENT-END TEMPERATURE PROBE PORT OF AN RT265 INFANT DUAL-HEATED EVAQUA2 BREATHING CIRCUIT DURING SETUP AND PRIOR TO PATIENT USE. THERE WAS NO REPORTED PATIENT CONSEQUENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23092699 ↗MalfunctionAug 28, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
A DISTRIBUTOR REPORTED ON BEHALF OF A HEALTHCARE FACILITY IN JAPAN, VIA A FISHER & PAYKEL (F&P) HEALTHCARE FIELD REPRESENTATIVE, THAT A 900MR869 TEMPERATURE/FLOW PROBE WAS IDENTIFIED TO BE EASILY DISLODGED FROM THE PATIENT-END TEMPERATURE PROBE PORT OF AN RT265 INFANT DUAL-HEATED EVAQUA2 BREATHING CIRCUIT DURING SETUP AND PRIOR TO PATIENT USE. THERE WAS NO REPORTED PATIENT CONSEQUENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22919470 ↗MalfunctionAug 24, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
A DISTRIBUTOR REPORTED ON BEHALF OF A HEALTHCARE FACILITY IN JAPAN, VIA A FISHER & PAYKEL (F&P) HEALTHCARE FIELD REPRESENTATIVE, THAT A 900MR869 TEMPERATURE/FLOW PROBE WAS IDENTIFIED TO BE EASILY DISLODGED FROM THE PATIENT-END TEMPERATURE PROBE PORT OF AN RT265 INFANT DUAL-HEATED EVAQUA2 BREATHING CIRCUIT DURING SETUP AND PRIOR TO PATIENT USE. THERE WAS NO REPORTED PATIENT CONSEQUENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22881666 ↗MalfunctionJul 31, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
A HEALTHCARE FACILITY IN COLORADO REPORTED VIA A FISHER & PAYKEL (F&P) HEALTHCARE FIELD REPRESENTATIVE THAT SEVEN 900MR869 TEMPERATURE/FLOW PROBES WERE FOUND DISLODGING FROM AN RT266 INFANT DUAL-HEATED EVAQUA2 BREATHING CIRCUIT DURING SET-UP AND PRIOR TO PATIENT USE. THERE WAS NO REPORTED PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22683612 ↗MalfunctionJun 12, 2025Connection Problem; Connection Problem
A DISTRIBUTOR IN PERU REPORTED THAT 39 900MR868 TEMPERATURE PROBES WERE IDENTIFIED TO HAVE A LOOSE CONNECTION WITH THE PATIENT-END TEMPERATURE PROBE PORTS OF BREATHING CIRCUITS. THERE WAS NO REPORTED PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22199977 ↗MalfunctionJun 8, 2025Loose or Intermittent Connection; Loose or Intermittent Connection
A HEALTHCARE FACILITY IN ILLINOIS REPORTED THAT A 900MR861 TEMPERATURE/FLOW PROBE WAS FOUND WITH A LOOSE CONNECTION TO A BREATHING CIRCUIT. THERE WAS NO REPORTED PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22164755 ↗MalfunctionMay 29, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
A DISTRIBUTOR REPORTED ON BEHALF OF A HEALTHCARE FACILITY IN JAPAN THAT THREE 900MR869 TEMPERATURE/FLOW PROBES WERE IDENTIFIED TO DISLODGE FROM THE PATIENT-END TEMPERATURE PROBE PORT OF AN INFANT BREATHING CIRCUIT PRIOR TO PATIENT USE. THERE WAS NO REPORTED PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22102877 ↗
Other Fisher & Paykel Healthcare Limited products
All Fisher & Paykel Healthcare Limited devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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