Recall Z-2271-2026— Covidien LLC

Name: FDA recall Z-2271-2026
Creator: U.S. Food and Drug Administration
Published: 2026-04-23

Class II · Ongoing

Class II FDA medical device recall by Covidien LLC, initiated 2026-04-23. FDA's recall record names no specific 510(k) clearance for this event. Product: Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF: 90042. Reason: Temperature probe devices lack FDA clearance..

Recalling firm: Covidien LLC
Classification: Class II
Status: Ongoing
Initiated: 2026-04-23
Firm location: Boulder, CO, United States

Product description

Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF: 90042

Reason for recall

Temperature probe devices lack FDA clearance.

Data sourced from openFDA. This site is unofficial and independent of the FDA.