{
  "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": "2026-09-05",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 3
    }
  },
  "results": [
    {
      "cfres_id": "220016",
      "product_res_number": "Z-2271-2026",
      "event_date_initiated": "2026-04-23",
      "event_date_posted": "2026-05-29",
      "recall_status": "Open, Classified",
      "res_event_number": "98859",
      "product_code": "BZT",
      "product_description": "Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM\nREF: 90042",
      "code_info": "UDI: 30884521820900/ Lot: 25D1267JZX\n25E1322JZX,\n25E1324JZX,\n25H0920JZX,",
      "firm_fei_number": "2936999",
      "recalling_firm": "Covidien LLC",
      "address_1": "6135 Gunbarrel Ave",
      "city": "Boulder",
      "state": "CO",
      "postal_code": "80301-3214",
      "additional_info_contact": "Technical and Clinical Support\n800-255-6774 Ext. 6",
      "reason_for_recall": "Temperature probe devices lack FDA clearance.",
      "root_cause_description": "Under Investigation by firm",
      "action": "On April 23, 2026 Covidien (subsidiary of Medtronic) issued a Urgent Medical Device Recall Notification to affected consignees via USPS. Covidien ask consignees to take the following actions: \n \n1. Quarantine all unused product from the affected lots.\n\n2. Return all unused product(s) from the affected lots in your inventory to Medtronic as described in the Customer Confirmation Form.\n\n3. Share this notice with all relevant personnel within your organization, and with any organization to which the potentially affected product from the specified lots has been transferred or distributed.\n\n4. Please complete and return the enclosed Customer Confirmation Form to rs.gmbmitgfca@medtronic.com even if you do not have unused inventory.",
      "product_quantity": "23,000 units",
      "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.",
      "openfda": {
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          "K062020",
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          "K862672",
          "K140134",
          "K864043",
          "K862131",
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        ],
        "registration_number": [
          "9613793",
          "2030624",
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          "2527072",
          "3003757840",
          "3003076831",
          "1928237",
          "1000521377",
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        ],
        "device_name": "Stethoscope, Esophageal, With Electrical Conductors",
        "medical_specialty_description": "Anesthesiology",
        "regulation_number": "868.1920",
        "device_class": "2"
      }
    }
  ]
}