{
  "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": "2026-06-03",
    "results": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Shoreview",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "98991",
      "recalling_firm": "IntegraDose Compounding Services LLC",
      "address_1": "3650 Victoria St N Ste 900",
      "address_2": "",
      "postal_code": "55126-2906",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "",
      "distribution_pattern": "Nationwide.",
      "recall_number": "D-0548-2026",
      "product_description": "fentaNYL Citrate, Sterile CADD for Injection, 2,2500 mcg/50mL in Sterile Water, IntegraDose Compounding Services LLC, 3650 Victorie St N, Suite 900, Shoreview, MN, NDC  71139-6030-1.",
      "product_quantity": "376 cassettes",
      "reason_for_recall": "Subpotent Drug",
      "recall_initiation_date": "20260512",
      "center_classification_date": "20260521",
      "report_date": "20260527",
      "code_info": "Lot#: 20260310FEN-1, Exp. Date: 09/06/2026",
      "more_code_info": ""
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}