{
  "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": "KOELN",
      "state": "N/A",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80430",
      "recalling_firm": "QIAGEN",
      "address_1": "19300 GERMANTOWN RD",
      "address_2": "GERMANTOWN MD 20874 USA",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic - MD  Internationally - AE, AU , CZ, DE, DZ, ES, FR, GB, HK , IE, IT, NO, RO & SA",
      "recall_number": "Z-2596-2018",
      "product_description": "EZ1 DSP Virus Kit (48), IVD, REF 62724 intended for in vitro diagnostic use.",
      "product_quantity": "287 pcs",
      "reason_for_recall": "Underfilled reagent well that could lead to incorrect results",
      "recall_initiation_date": "20180528",
      "center_classification_date": "20180802",
      "termination_date": "20190405",
      "report_date": "20180808",
      "code_info": "UDI - 04053228000099  Lot - 160020069  Expiration - 11/01/19"
    }
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}