{
  "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": "200 bags",
      "code_info": "Lot # 5/23/18 3812 89325P, BUD 8/6/2018.",
      "center_classification_date": "20180719",
      "distribution_pattern": "Nationwide in the USA",
      "state": "AZ",
      "product_description": "PHENYLephrine 40 mg (PHENYLephrine HCL (USP) 40 mg, 5%Dextrose Inj., USP 250 mL) Volume: 254 mL. Single dose bag. Avella of Houston, 9265 Kirby Dr., Houston, TX 77054. NDC 42852-893-25",
      "report_date": "20180725",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Avella of Deer Valley, Inc. Store 38",
      "recall_number": "D-0940-2018",
      "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"
    }
  ]
}