{
  "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": "2026-10-14",
    "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": "99799",
      "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": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the state of NJ and the countries of Azerbaijan, Belgium, Czech Republic, Germany, Hungary, India, Italy, Kuwait, Russia, Spain, Ukraine.",
      "recall_number": "Z-0082-2027",
      "product_description": "Sperm Ab ELISA;  Model/Catalog Number: EIA-1826;  Product Description: Sperm Ab ELISA (96 well plate test);",
      "product_quantity": "211",
      "reason_for_recall": "Potential for false negative patient results.",
      "recall_initiation_date": "20260702",
      "center_classification_date": "20261002",
      "report_date": "20261014",
      "code_info": "Model/Catalog Number: EIA-1826; UDI: 04048474018264; Lot# 320K046;"
    }
  ]
}