{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Elkton",
      "state": "MD",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82212",
      "recalling_firm": "Terumo Medical Corporation",
      "address_1": "950 Elkton Blvd",
      "address_2": "N/A",
      "postal_code": "21921-5322",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "The products were distributed to the following US states: FL, IN, KS, KY, MA, MO, NH, NV, PA, SC, TN, and TX.",
      "recall_number": "Z-2005-2019",
      "product_description": "Terumo Needle, 23G x 1\", Product Code NN2325R",
      "product_quantity": "30,000",
      "reason_for_recall": "There is a potential for a loss of package integrity that may compromise the sterility of the product.",
      "recall_initiation_date": "20190208",
      "center_classification_date": "20190722",
      "termination_date": "20200508",
      "report_date": "20190731",
      "code_info": "Lot Numbers 180811C"
    }
  ]
}