{
  "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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    {
      "status": "Terminated",
      "city": "Columbus",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "74135",
      "recalling_firm": "Profarma Distributors LLC",
      "address_1": "4751 Poth Rd",
      "address_2": "N/A",
      "postal_code": "43213-1331",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-1042-2016",
      "product_description": "VERMOX Tablets 500 mg, 1-count box, UPC 501109900596",
      "product_quantity": "254 boxes (254 tablets)",
      "reason_for_recall": "CGMP Deviations",
      "recall_initiation_date": "20160511",
      "center_classification_date": "20160617",
      "termination_date": "20170124",
      "report_date": "20160629",
      "code_info": "Lot # UJE 040; Exp. 02/17"
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}