{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Springfield",
      "state": "NJ",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97196",
      "recalling_firm": "DRG International, Inc.",
      "address_1": "841 Mountain Ave",
      "address_2": "N/A",
      "postal_code": "07081-3437",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of CA, MA, PA and the countries of  Germany, Hong Kong, Moldova.",
      "recall_number": "Z-2265-2025",
      "product_description": "Brand Name: T4 Total ELISA  Product Name: T4 Total ELISA  Model/Catalog Number: EIA-4568  Product Description: T4 Total ELISA",
      "product_quantity": "47 units",
      "reason_for_recall": "An incoming complaint reported that the expiration date on the kit box label and Certificate of Analysis (CoA) exceeded the shelf life of the standards and control solutions in the kit by 2 months (i.e., 2026-03-31 instead of 2026-01-31). The expiration dates on the bottle labels were correct (i.e., 2026-01-31).",
      "recall_initiation_date": "20250604",
      "center_classification_date": "20250804",
      "report_date": "20250813",
      "code_info": "Model/Catalog Number: EIA-4568; UDI-DI: 04048474045680; Lot number: 304K034;",
      "more_code_info": ""
    }
  ]
}