{"url_path":"/fda/device/recalls/Z-2271-2026","section_key":"summary","section_title":"DEVICE Recall: Covidien LLC — Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM  REF: 90042","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-04-23","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2271-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Covidien LLC"},"word_count":95,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2271-2026\n\n**Recalling firm:** Covidien LLC\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-04-23\n**Report date:** 2026-06-10\n\n## Product\nCovidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM  REF: 90042\n\n## Reason\nTemperature probe devices lack FDA clearance.\n\n## Affected lots\nUDI: 30884521820900/ Lot: 25D1267JZX 25E1322JZX, 25E1324JZX, 25H0920JZX,\n\n## Distribution\nUS 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."}