Class II
Medical Device Recall: Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF: 90042
Covidien LLC · April 23, 2026
Reason for Recall
Temperature probe devices lack FDA clearance.
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.
States Affected
NATIONWIDE
Quantity Affected
23,000 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2271-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.