{
  "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": [
    {
      "country": "United States",
      "city": "Columbus",
      "address_1": "2550 John Glenn Ave Ste A",
      "reason_for_recall": "Labeling: Label Mix-Up: A typographical error in the product form on the carton label incorrectly lists the configuration as 30 \"Capsules\" (3 x 10) rather than \"Tablets\".",
      "address_2": "",
      "product_quantity": "1,170 cartons",
      "code_info": "Lot #: 113032A, 113032B, Exp 04/13",
      "center_classification_date": "20120814",
      "distribution_pattern": "Nationwide",
      "state": "OH",
      "product_description": "Topiramate Tablets, 50 mg, 30-count (3 x 10) unit-dose blisters per carton, Rx only, Mfd by: Cadila Healthcare Ltd., Ahmedabad, India; Dist By: Zydus Pharmaceuticals USA, Inc., Pennington, NJ 08534, Pkg by: American Health Packaging, Col. OH 43217, NDC 68084-343-21, blister barcode 6808434311",
      "report_date": "20120822",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "American Health Packaging",
      "recall_number": "D-1645-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "62792",
      "termination_date": "20130702",
      "more_code_info": "",
      "recall_initiation_date": "20120725",
      "postal_code": "43217-1188",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}