{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "105007",
      "product_res_number": "Z-0372-2012",
      "event_date_initiated": "2011-09-26",
      "event_date_posted": "2012-01-11",
      "recall_status": "Terminated",
      "event_date_terminated": "2013-08-13",
      "res_event_number": "60307",
      "product_code": "BZT",
      "k_numbers": [
        "K072621"
      ],
      "product_description": "Cincinnati Sub Zero,  Steri-Probe Temperature Probe, Esophageal/Rectal Temperature Probe, Part Number:  39622, Catalog #491B.  TA disposable temperature probe used in conjunction with a measuring/monitoring device to continuously measure/monitor a patient's core body temperature.",
      "code_info": "The following lot codes are subject to recall:  12998, 12999, 19257, 19257A, 19644, 21536, 21537, 27446, 29112, 31081, 31082, 32209, 37281, 38522,  8996, D414723, D416607, D420120, D421702, D423801, D423908, D525212, D515408, D516607, D517108, D520709, D524107, D525502, D527632, D530518, D624011, D624012, D634834\n\n D706611, D709119, D720450, D721118, D722015, and D727416.",
      "firm_fei_number": "1516825",
      "recalling_firm": "Cincinnati Sub-Zero Products Inc",
      "address_1": "12011 Mosteller Rd",
      "city": "Cincinnati",
      "state": "OH",
      "postal_code": "45241",
      "additional_info_contact": "Beatrice Washington\n513-772-8810",
      "reason_for_recall": "Reports that the Rectal/ Esophageal Temperature Probes are not reading correctly. This situation causes the Blanketrol device, which the probes connect to, to shut down operation and display a 'check probe' error.",
      "root_cause_description": "Nonconforming Material/Component",
      "action": "Cincinnati Sub-Zero Products, Inc., issued an \"Urgent Medical Device Field Action\" letter on November 1, 2011 to all affected customers. The letter includes; description of product and problem,  and a list of the affected lot numbers. The letter instructs the customers to discontinue use of the device. All unused product is to be returned to the Biomedical/Clinical Engineering and/or Service Department for an replacement and all used probes are to be disposed of in accordance with hospital policy. The customers are also instructed to complete and return an attached Recall Response Form ASAP. For additional information, customers may contact the Beatrice Washington at 1-800-989-7373 or (513) 772-8810.",
      "product_quantity": "369,680",
      "distribution_pattern": "Nationwide distribution and Canada.",
      "openfda": {
        "k_number": [
          "K953793",
          "K870255",
          "K881293",
          "K864858",
          "K930533",
          "K812976",
          "K841098",
          "K821890",
          "K973839",
          "K894757",
          "K852228",
          "K811862",
          "K843071",
          "K925789",
          "K943495",
          "K810147",
          "K940169",
          "K882319",
          "K092716",
          "K982193",
          "K864043",
          "K904943",
          "K874295",
          "K111050",
          "K830716",
          "K873344",
          "K961060",
          "K893409",
          "K854212",
          "K072621",
          "K823743",
          "K885347",
          "K844055",
          "K862131",
          "K842309",
          "K251025",
          "K811928",
          "K062020",
          "K193027",
          "K862672",
          "K862548",
          "K861541",
          "K930929",
          "K791190",
          "K140134",
          "K922007"
        ],
        "registration_number": [
          "2936999",
          "2432320",
          "1055236",
          "2030624",
          "2032112",
          "2025816",
          "3018094310",
          "1054241",
          "9681384",
          "2032273",
          "3007007790",
          "9613793",
          "3003915875",
          "1927197",
          "1928237",
          "3006845683",
          "9617604",
          "3006845687",
          "1043214",
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          "8022257",
          "2246552",
          "3023031046",
          "2527072"
        ],
        "fei_number": [
          "2936999",
          "1000521377",
          "3003076831",
          "2025816",
          "3018094310",
          "3003240904",
          "3002558692",
          "3007007790",
          "3003915875",
          "1927197",
          "1928237",
          "3006845683",
          "3006845687",
          "3003757840",
          "1043214",
          "1000112877",
          "1721686",
          "2246552",
          "1000112968",
          "3000206435",
          "3023031046",
          "2527072",
          "3002807626",
          "3006469671"
        ],
        "device_name": "Stethoscope, Esophageal, With Electrical Conductors",
        "medical_specialty_description": "Anesthesiology",
        "regulation_number": "868.1920",
        "device_class": "2"
      }
    }
  ]
}