{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Little Rock",
      "address_1": "8821 Knoedl Ct",
      "reason_for_recall": "Lack of assurance of sterility: Product bags leaking at seam.",
      "address_2": "",
      "product_quantity": "87 bags",
      "code_info": "LOT # 20170505@23, 20170505@28, Use By: 08/03/17",
      "center_classification_date": "20170531",
      "distribution_pattern": "Nationwide in the USA",
      "state": "AR",
      "product_description": "HYDROmorphone HCL in 0.9% Sodium Chloride injectable, 0.2 mg per ml, Total Volume 100mL, Single Dose Container bag, (Total HYDROmorphone Dose 20 mg per 100 mL) Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0300-55",
      "report_date": "20170607",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "SCA Pharmaceuticals",
      "recall_number": "D-0875-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "77314",
      "termination_date": "20180329",
      "more_code_info": "",
      "recall_initiation_date": "20170518",
      "postal_code": "72205-4600",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}