{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-06-24",
    "results": {
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    {
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      "city": "Boulder",
      "state": "CO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98859",
      "recalling_firm": "Covidien LLC",
      "address_1": "6135 Gunbarrel Ave",
      "address_2": "",
      "postal_code": "80301-3214",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "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.",
      "recall_number": "Z-2272-2026",
      "product_description": "Covidien Mon-a-Therm General Purpose Temperature Probe  REF: 90044",
      "product_quantity": "1775 units",
      "reason_for_recall": "Temperature probe devices lack FDA clearance.",
      "recall_initiation_date": "20260423",
      "center_classification_date": "20260529",
      "report_date": "20260610",
      "code_info": "UDI: 30884521828388/ Lot: 25F0945JZX 25H0949JZX, 25I1065JZX, 25I1066JZX",
      "more_code_info": ""
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}