{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Marburg",
      "state": "",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80575",
      "recalling_firm": "DRG Instruments GmbH",
      "address_1": "Frauenbergstr. 18",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "NJ; Germany, Belgium, Spain & Germany",
      "recall_number": "Z-2836-2018",
      "product_description": "Salivary Estradiol ELISA, REF SLV-4188 in vitro diagnostic quantitative measurement of active free Estradiol, an estrogenic steroid, in saliva.",
      "product_quantity": "169 kits",
      "reason_for_recall": "Lower recovery of salivary estradiol levels due to poor differentiation between kit Standard 0 and Standard 1.",
      "recall_initiation_date": "20160714",
      "center_classification_date": "20180816",
      "termination_date": "20200804",
      "report_date": "20180822",
      "code_info": "Lot # 68K056  Exp. Date 2017-05",
      "more_code_info": ""
    }
  ]
}