{
  "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,
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  "results": [
    {
      "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-1041-2016",
      "product_description": "VERMOX Tablets 100 mg; 6-count box, UPC 7501109900619",
      "product_quantity": "163 boxes (978 tablets)",
      "reason_for_recall": "CGMP Deviations",
      "recall_initiation_date": "20160511",
      "center_classification_date": "20160617",
      "termination_date": "20170124",
      "report_date": "20160629",
      "code_info": "Lot # UPE187; Exp. 08/17"
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}