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Mon-a-Therm 90049Recalls & reported problems

Covidien LP · Esophageal Stethoscope with Temperature Sensor 400TM · Class 2

All models of Mon-a-Therm (12)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20884521031743), received between Feb 4, 2019 and Feb 4, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Low Readings” (1 report).

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 18, 2026.

Most reported problems

Device problems

  • Low Readings1

Patient problems

  • No Information1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionFeb 4, 2019Low Readings; Low Readings

    ACCORDING TO THE REPORTER, THE UNIT FAILED TO INTERFACE CORRECTLY WITH OTHER DEVICE LEADING IN A TEMPERATURE COOLER THAT THE SET PATIENT'S TEMPERATURE. IT WAS STATED THAT THEY SWITCH OFF THE OTHER DEVICE BUT THE PATIENT'S TEMPERATURE DID NOT RISE. THERE WAS NO REPORTED PATIENT OUTCOME.

    Patient problems: No Information

    MAUDE report 8300909 ↗

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Sources and updates

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