{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Guilford",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91300",
      "recalling_firm": "Detect Headquarters",
      "address_1": "351 New Whitfield St",
      "address_2": "N/A",
      "postal_code": "06437-3400",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Domestic distribution nationwide. Foreign distribution to Hong Kong.",
      "recall_number": "Z-0879-2023",
      "product_description": "Detect Covid-19 Test  Product/Model Number: 21205",
      "product_quantity": "10142 (US); 960 OUS",
      "reason_for_recall": "There is an increased chance that the tests from affected lots may give false negative results. Health risks resulting from a false negative result include delay or lack of supportive treatment and lack of monitoring of infected individuals and their household or other close contacts for symptoms resulting in increased risk of spread of COVID-19 within the community.",
      "recall_initiation_date": "20221208",
      "center_classification_date": "20230104",
      "report_date": "20230111",
      "code_info": "HY263, HY264, and HB264  Expiration 01JAN2023"
    }
  ]
}