{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Franklin",
      "state": "KY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "67739",
      "recalling_firm": "Blu Pharmaceuticals Inc",
      "address_1": "301 Robey St",
      "address_2": "N/A",
      "postal_code": "42134-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "NJ, UT, IL and CT",
      "recall_number": "D-1302-2014",
      "product_description": "Metformin Hydrochloride Tablets USP 1000 mg, 500 tablets Rx Only, Manufactured by Blu Caribe Dorado PR 00646. Distributed by Blu Pharmaceuticals Franklin NY 42134, NDC  24658-0292-05",
      "product_quantity": "101,500 tablets",
      "reason_for_recall": "Defective container: Product distributed without inner seal on bottles.",
      "recall_initiation_date": "20140313",
      "center_classification_date": "20140505",
      "termination_date": "20150610",
      "report_date": "20140514",
      "code_info": "Lot # 13E0014F1P8V; Exp. 04/15"
    }
  ]
}