{
  "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": "Livonia",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "71454",
      "recalling_firm": "The Harvard Drug Group, LLC",
      "address_1": "31778 Enterprise Dr",
      "address_2": "",
      "postal_code": "48150-1960",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-1150-2015",
      "product_description": "OXYCODONE HCl C-II Tablets, 5 mg USP, 100-count blister cards, Rx only, Manufactured by Nesher Pharmaceuticals USA LLC., St. Louis, MO 63044, Distributed by Major Pharmaceuticals, Livonia, MI 48150, NDC 0904-6444-61.",
      "product_quantity": "12,717 tablets",
      "reason_for_recall": "Superpotent Drug: Confirmed customer complaint of a single unit dose blister cavity containing 2 OXYCODONE HCl 5 mg tablets.",
      "recall_initiation_date": "20150610",
      "center_classification_date": "20150629",
      "termination_date": "20160912",
      "report_date": "20150708",
      "code_info": "Lot # P-20000;  Exp. 08/16  Lot # P-20004;  Exp. 08/16",
      "more_code_info": ""
    }
  ]
}