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Covidien Mon-a-Therm Esophageal Stethoscope
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MEDICAL DEVICE RECALLMODERATE

Covidien Mon-a-Therm Esophageal Stethoscope

Covidien is recalling Mon-a-Therm Esophageal Stethoscopes with Temperature Sensors because the devices lack FDA clearance.

What to do

Stop using the affected temperature probe devices and contact the manufacturer for further instructions.

Posted
Updated
Agency
Firm
Covidien LLC
Recall ID
98859
Status
ONGOING

Why it was recalled

Temperature probe devices lack FDA clearance.

How to identify it

Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM

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Editorial summary by Recall Canary · last updated 2026-05-30 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification