{
  "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,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Houston",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "82718",
      "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": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide in the US",
      "recall_number": "D-1251-2019",
      "product_description": "HYDROmorphone 20 mg/100 mL Injectable Solution, Hydromorphone HCl 20 mg 0.9% Sodium Chloride 100 mL, Sterile single use bag, Compounded Drug, Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404, NDC: 42852-221-10",
      "product_quantity": "560 bags",
      "reason_for_recall": "Sub-potency",
      "recall_initiation_date": "20190426",
      "center_classification_date": "20190429",
      "termination_date": "20191030",
      "report_date": "20190508",
      "code_info": "Lot: 01/14/19 0215 22110P Exp. 04/29/2019"
    }
  ]
}