{
  "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,
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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-0060-2018",
      "product_description": "HYDROmorphone HCL 1 mg per mL in 0.9% Sodium Chloride 25 mL Fill in 30 mL single-dose syringe (Total Dose Hydromorphone 25 mg/25 mL)  Rx Only SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR NDC 70004-0303-17",
      "product_quantity": "128 syringes",
      "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: 20170808@52 BUD: 11/06/2017"
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}