{
  "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": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Little Rock",
      "state": "AR",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "78320",
      "recalling_firm": "SCA Pharmaceuticals, LLC",
      "address_1": "8821 Knoedl Ct",
      "address_2": "N/A",
      "postal_code": "72205-4600",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the United States",
      "recall_number": "D-0061-2018",
      "product_description": "HYDROmorphone HCl 20 mcg / mL BUPIvacaine HCl 0.075% in 0.9% Sodium Chloride 50 mL (HYDROmorphone Total Dose 1000 mcg) Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-0331-22",
      "product_quantity": "60 bags",
      "reason_for_recall": "Lack Of Assurance Of Sterility.",
      "recall_initiation_date": "20171019",
      "center_classification_date": "20171102",
      "termination_date": "20190501",
      "report_date": "20171108",
      "code_info": "Lot: 20170816@65 BUD: 10/30/2017"
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