{
  "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": "Ongoing",
      "city": "Springfield",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88949",
      "recalling_firm": "DRG International, Inc.",
      "address_1": "841 Mountain Ave",
      "address_2": "",
      "postal_code": "07081-3437",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Domestic: NY; International: TZ, VN, BD, CO, TT, YE, BO, DE, SV, GE, PY, TG, RU/UA, NI, DO, NG, EG & CM",
      "recall_number": "Z-0310-2022",
      "product_description": "Total Thyroxine (T4) ELISA; REF EIA-1781",
      "product_quantity": "314 total (270 US)",
      "reason_for_recall": "Firm has identified two lots of product that do not meet product shelf life, resulting in failed Controls. The clinical impact may be a delay in diagnosis and a consumption of patient samples.",
      "recall_initiation_date": "20211018",
      "center_classification_date": "20211129",
      "report_date": "20211208",
      "code_info": "lot#: RN-60923 expiration date 12/31/2021; RN-60831 expiration date 12/31/2021",
      "more_code_info": ""
    }
  ]
}