{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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  "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": "100 cassettes",
      "code_info": "Lot #: 5/14/18 1012 172-27886Y, BUD 6/28/2018.",
      "center_classification_date": "20180719",
      "distribution_pattern": "Nationwide in the USA",
      "state": "AZ",
      "product_description": "fentaNYL 2 mcg/mL,  0.125% ROPivacaine, Fentanyl Citrate, USP 300 mcg, Ropivacaine HCL PF, USP 187.5 mg, 0.9% Sodium Chloride, USP QS 150 mL. Volume: 150 mL. Single dose cassette For: Methodist Dallas Medical Center. By: Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054. NDC 15082-278-86",
      "report_date": "20180725",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Avella of Deer Valley, Inc. Store 38",
      "recall_number": "D-0946-2018",
      "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"
    }
  ]
}