{
  "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": [
    {
      "status": "Terminated",
      "city": "Phoenix",
      "state": "AZ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "81413",
      "recalling_firm": "Avella of Deer Valley, Inc. Store 38",
      "address_1": "24416 N 19th Ave",
      "address_2": "N/A",
      "postal_code": "85085-1887",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.A. nationwide.",
      "recall_number": "D-0135-2019",
      "product_description": "Phenylephrine 30 mg added to NS 250 mL Bag, Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, and Avella of Deer Valley, Inc. #38",
      "product_quantity": "300 bags",
      "reason_for_recall": "Lack of assurance of sterility",
      "recall_initiation_date": "20181019",
      "center_classification_date": "20181101",
      "termination_date": "20210506",
      "report_date": "20181107",
      "code_info": "Lot# 138-20180409@55, Exp 11/18/2018"
    }
  ]
}