{
  "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": [
    {
      "country": "United States",
      "city": "Houston",
      "address_1": "9265 Kirby Dr",
      "reason_for_recall": "Subpotent Drug: final drug concentration is subpotent as compared to the concentration indicated on the label.",
      "address_2": "",
      "product_quantity": "100 syringes",
      "code_info": "Lot #: 6/12/18 0432 149-21072S, BUD 9/10/18",
      "center_classification_date": "20180625",
      "distribution_pattern": "Distributed to one medical center in Fort Worth, TX.",
      "state": "TX",
      "product_description": "fentanyl Citrate USP 5 mcg in 0.9% Sodium Chloride USP 0.5 mL, 10 mcg per mL prefilled syringe, Rx only, Advanced Pharma an FDA Regulated 503B Outsourcing Facility 9265 Kirby Dr., Houston, TX  77054, NDC 15082-210-72.",
      "report_date": "20180704",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Advanced Pharma Inc.",
      "recall_number": "D-0889-2018",
      "initial_firm_notification": "Telephone",
      "product_type": "Drugs",
      "event_id": "80354",
      "termination_date": "20190403",
      "more_code_info": "",
      "recall_initiation_date": "20180620",
      "postal_code": "77054-2520",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}