{"url_path":"/fda/device/recalls/Z-2272-2026","section_key":"summary","section_title":"DEVICE Recall: Covidien LLC — Covidien Mon-a-Therm General Purpose Temperature Probe  REF: 90044","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-2272-2026%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":93,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2272-2026\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 General Purpose Temperature Probe  REF: 90044\n\n## Reason\nTemperature probe devices lack FDA clearance.\n\n## Affected lots\nUDI: 30884521828388/ Lot: 25F0945JZX 25H0949JZX, 25I1065JZX, 25I1066JZX\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."}