{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Phoenix",
      "address_1": "24416 N 19th Ave",
      "reason_for_recall": "Lack of Assurance of Sterility: Potential leakage of bags.",
      "address_2": "",
      "product_quantity": "660 bags",
      "code_info": "Lot #: 4/26/18 0520 22110P, BUD 8/9/2018; 5/14/18 1350 22110P, BUD 8/27/2018.",
      "center_classification_date": "20180719",
      "distribution_pattern": "Nationwide in the USA",
      "state": "AZ",
      "product_description": "HYDROmorphone 0.2mg/mL. (Hydromorphone HCL (USP) 20 mg, 0.9% Sodium Chloride (USP) QS 100 mL) Volume: 100mL. Single dose bag. Advanced Pharma, 9265 Kirby Dr., Houston,077054 TX. NDC 15082-221-10",
      "report_date": "20180725",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Avella of Deer Valley, Inc. Store 38",
      "recall_number": "D-0950-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "80307",
      "termination_date": "20200124",
      "more_code_info": "",
      "recall_initiation_date": "20180612",
      "postal_code": "85085-1887",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}