{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Phoenix",
      "address_1": "24416 N 19th Ave",
      "reason_for_recall": "Lack of Assurance of Sterility",
      "address_2": "",
      "product_quantity": "911 syringes",
      "code_info": "Lot # 138-20182408@58 BUD 12/22/2018",
      "center_classification_date": "20181107",
      "distribution_pattern": "Product was distributed throughout the United States.",
      "state": "AZ",
      "product_description": "BEVACIZUMAB 2.5 MG/0.1ML, pre-filled syringe (deliverable dose of 1.25MG in normject syringe) Repackaged by Avella Specialty Pharmacy, 24416 N 19th Avenue, Pheonix, AZ 85085. NDC 42852-001-24",
      "report_date": "20181114",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Avella of Deer Valley, Inc. Store 38",
      "recall_number": "D-0224-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "81466",
      "termination_date": "20190118",
      "more_code_info": "",
      "recall_initiation_date": "20181031",
      "postal_code": "85085-1887",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}