{
  "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,
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "Germantown",
      "state": "MD",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87205",
      "recalling_firm": "Qiagen Sciences LLC",
      "address_1": "19300 Germantown Rd",
      "address_2": "",
      "postal_code": "20874-1415",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Other",
      "distribution_pattern": "Domestic: AZ, CA, DC, CO,FL,HI, IL,  KY, MI, MO, NC, NJ, NM, NY, OH, RI, TX, WA, WY",
      "recall_number": "Z-0941-2021",
      "product_description": "SARS-CoV-2 Antigen Test",
      "product_quantity": "1092 boxes of 60 (65,520 e-sticks)",
      "reason_for_recall": "QIAGEN has become aware of the potential for false positive results to occur with some patient samples.",
      "recall_initiation_date": "20210115",
      "center_classification_date": "20210131",
      "termination_date": "20220711",
      "report_date": "20210210",
      "code_info": "GTIN: 04053228039785, Catalog #: 646533,  Lot #: 86651, 86652, 86653, 86654, 86659.",
      "more_code_info": ""
    }
  ]
}