{
  "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": "Lake Forest",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "70743",
      "recalling_firm": "Akorn, Inc.",
      "address_1": "1925 W. Field Court, Suite 300",
      "address_2": "N/A",
      "postal_code": "60045",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide and Puerto Rico",
      "recall_number": "D-0995-2015",
      "product_description": "SULFAMETHOXAZOLE AND TRIMETHOPRIM ORAL SUSPENSION, USP,200 mg/ 40 mg per 5mL, CHERRY FLAVOR, 16 fl oz (473 mL) bottles (NDC 50383-0823-16), Rx only, HI-TECH PHARMACAL CO. INC, Amityville, NY 11701",
      "product_quantity": "27,648 bottles (16 fl. oz. each)",
      "reason_for_recall": "Failed Dissolution Specifications: Out of specification for dissolution of sulfamethoxazole.",
      "recall_initiation_date": "20150317",
      "center_classification_date": "20150508",
      "termination_date": "20171227",
      "report_date": "20150520",
      "code_info": "Lot # 623940, Exp. 10/2015;  Lot # 624487, Exp. 11/2015;  Lot # 624741, Exp. 11/2015;  Lot # 625296, Exp. 1/2016",
      "more_code_info": ""
    }
  ]
}