Mon-a-Therm 90044 (UDI 20884521031590)Recalls & reported problems
Covidien LP · General Purpose Temperature Probe 400TM · Class 2
All models of Mon-a-Therm (12)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 20884521031590), received between Jan 7, 2019 and Apr 18, 2024 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Low Readings” (3 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, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Low Readings3
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 18, 2024Low Readings; Low Readings
ACCORDING TO THE REPORTER, THE TEMPERATURE PROBE WAS IN PLACE FOR 48 HOURS. AFTER REMOVAL FOR INTIMATE WASHING, REINSTALLATION OF THE DEVICE. MALFUNCTION WITH TEMPERATURE DIFFERENCE OF UP TO 2 DEGREES LESS THAN THE SOCKET TYMPANIC. CHANGING THE PROBE, USING THE SAME REFERENCE, THE SAME BATCH AND IT HAD SIMILAR PROBLEM. THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19136809 ↗MalfunctionApr 17, 2024Low Readings; Low Readings
ACCORDING TO THE REPORTER, THE TEMPERATURE PROBE WAS IN PLACE FOR 48 HOURS. AFTER REMOVAL FOR INTIMATE WASHING, REINSTALLATION OF THE DEVICE. MALFUNCTION WITH TEMPERATURE DIFFERENCE OF UP TO 2 DEGREES LESS THAN THE SOCKET TYMPANIC. CHANGING THE PROBE, USING THE SAME REFERENCE, THE SAME BATCH AND IT HAD SIMILAR PROBLEM. THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19126918 ↗MalfunctionJan 7, 2019Low Readings; Low Readings
ACCORDING TO THE REPORTER, DURING PROCEDURE, THE UNIT'S READING WAS LOWER THAN MANUAL MONITORING. THERE WAS NO PATIENT INJURY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8224340 ↗
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- CARESCAPE B450 MBA313GE Healthcare Finland Oy · Thermometer, electronic, clinical1 recall1 report
- Temperature Probes Esophageal/Rectal Temperature ProbePhilips Medical Systems Hsg · Thermometer, electronic, clinical1 recall1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- 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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