{
  "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": "Houston",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "82398",
      "recalling_firm": "Advanced Pharma Inc.",
      "address_1": "9265 Kirby Dr",
      "address_2": "N/A",
      "postal_code": "77054-2520",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-1018-2019",
      "product_description": "fentaNYL 2500 mcg/250 mL Injectable Solution, Fentanyl 0.9% Sodium Chloride, QS, Sterile single use bags, NDC: 42852-210-25 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404",
      "product_quantity": "180 bags",
      "reason_for_recall": "Lack of Assurance of Sterility",
      "recall_initiation_date": "20190313",
      "center_classification_date": "20190321",
      "termination_date": "20200114",
      "report_date": "20190327",
      "code_info": "Lot: 01/03/19 1645 21025P Exp. 5/3/2019"
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}