{
  "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": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Doral",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87300",
      "recalling_firm": "Sky Medical Supplies and Equipments LLC",
      "address_1": "5987 Nw 102nd Ave",
      "address_2": "N/A",
      "postal_code": "33178-2820",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the state of Florida and the country of Peru.",
      "recall_number": "Z-1127-2021",
      "product_description": "AntIbody to SARS-CoV-2 - Product Usage: (Colloidal Gold) for IgG/IgM Diagnostic Kit, RAPID TEST DEVICE, Whole Blood/Serum/Plasma, SKY Medical Supplies and Equipments, LLC.",
      "product_quantity": "10,000 kits",
      "reason_for_recall": "Distributed COVID test kits without emergency use authorization.",
      "recall_initiation_date": "20210119",
      "center_classification_date": "20210216",
      "termination_date": "20260310",
      "report_date": "20210224",
      "code_info": "2020042901"
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}