{
  "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": "Loveland",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86798",
      "recalling_firm": "VEO DIAGNOSTICS, LLC",
      "address_1": "422 Wards Corner Rd",
      "address_2": "N/A",
      "postal_code": "45140-6964",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution including in the states of IA, PA, WA.",
      "recall_number": "Z-0510-2021",
      "product_description": "ACCEL ELISA COVID-19 for the detection of total antibodies to SARS-CoV-2  Catalog AE301U    Kit lots: PXCOV073020, PXCOV081220  Expiration dates: January 18, 2021 and January 26, 2021",
      "product_quantity": "15 kits",
      "reason_for_recall": "Emergency Use Authorization (EUA) removed from list of COVID-19 antibody tests",
      "recall_initiation_date": "20201105",
      "center_classification_date": "20201201",
      "termination_date": "20210416",
      "report_date": "20201209",
      "code_info": "Kit lots: PXCOV073020, PXCOV081220  Expiration dates: January 18, 2021 and January 26, 2021",
      "more_code_info": ""
    }
  ]
}