Covidien Llc: Stethoscope, Esophageal, With Electrical Conductors
Recall Summary Covidien is recalling Mon-a-Therm Esophageal Stethoscopes with Temperature Sensors (model 400TM, REF 90042) distributed nationwide because the temperature probe component lacks required FDA clearance. This Class II recall affects medical devices that may have been used in hospitals and healthcare facilities across the United States.
- Recalling firm
- Covidien LLC
- Product
- Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF: 90042
- Reason
- Temperature probe devices lack FDA clearance.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-04-23
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, FL, GA, HI, IL, LA, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NY, OH, OK, OR, PA, PR, TN, TX, UT, VA, WA, WV.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/097ea159-0925-43ea-a819-6e0bba06882b