{
  "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": "740 syringes",
      "code_info": "Lot #:2/26/18 2233 24363M, BUD 6/26/2018.",
      "center_classification_date": "20180719",
      "distribution_pattern": "Nationwide in the USA",
      "state": "AZ",
      "product_description": "MORphine 150 mg (Morphine Sulfate, USP 150mg in 0.9% Sodium Chloride, USP QS 30mL). Volume 30 mL. Single dose syringe. Avella of Houston, 9265 Kirby Dr., Houston, TX 77054. NDC 42852-243-63",
      "report_date": "20180725",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Avella of Deer Valley, Inc. Store 38",
      "recall_number": "D-0954-2018",
      "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"
    }
  ]
}