Mon-a-Therm 90042Recalls & reported problems
Covidien LP · Esophageal Stethoscope with Temperature Sensor 400TM · Class 2
All models of Mon-a-Therm (12)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
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.
Recalls naming this device
- Apr 23, 2026Open, Classified
Temperature probe devices lack FDA clearance.
Z-2271-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Other STETHOSCOPE, ESOPHAGEAL, WITH ELECTRICAL CONDUCTORS devices
- DeRoyal 81-040412Deroyal Industries, Inc. · STETHOSCOPE, ESOPHAGEAL, WITH ELECTRICAL CONDUCTORS3 reports
- DeRoyal 81-040418Deroyal Industries, Inc. · STETHOSCOPE, ESOPHAGEAL, WITH ELECTRICAL CONDUCTORS3 reports
- Medline DYNJAER4009Medline Industries, Inc. · STETHOSCOPE, ESOPHAGEAL, WITH ELECTRICAL CONDUCTORS2 reports
- DeRoyal 81-040409Deroyal Industries, Inc. · STETHOSCOPE, ESOPHAGEAL, WITH ELECTRICAL CONDUCTORS1 report
- Level 1 ES400-18Icu Medical, Inc. · STETHOSCOPE, ESOPHAGEAL, WITH ELECTRICAL CONDUCTORS1 report
- DeRoyal 81-050418Deroyal Industries, Inc. · STETHOSCOPE, ESOPHAGEAL, WITH ELECTRICAL CONDUCTORS1 report
- Mon-a-Therm 90049Covidien LP · STETHOSCOPE, ESOPHAGEAL, WITH ELECTRICAL CONDUCTORS1 report
- DeRoyal 81-050409Deroyal Industries, Inc. · STETHOSCOPE, ESOPHAGEAL, WITH ELECTRICAL CONDUCTORS1 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
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- 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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