{
  "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": "Completed",
      "city": "Pompano Beach",
      "state": "FL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89315",
      "recalling_firm": "Empowered Diagnostics LLC",
      "address_1": "3341 W Mcnab Rd",
      "address_2": "N/A",
      "postal_code": "33069-4808",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-0481-2022",
      "product_description": "ImmunoPass , COVID-19 Neutralizing Antibody Test, NAB 900-60",
      "product_quantity": "2100 units",
      "reason_for_recall": "COVID test kits were offered for sale and distributed to consumers in the United States without marketing approval, clearance, or authorization from FDA.",
      "recall_initiation_date": "20211222",
      "center_classification_date": "20220128",
      "report_date": "20220209",
      "code_info": "all lots"
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}