{
  "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": "82615",
      "recalling_firm": "Customceutical Compounding",
      "address_1": "4611 E Shea Blvd Bldg 3 Ste 180",
      "address_2": "N/A",
      "postal_code": "85028-4258",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "U.S.A. Nationwide",
      "recall_number": "D-1258-2019",
      "product_description": "Test D (TESTOSTERONE CYPIONATE 200MG/ML VITAMIN D3 5,000IU/ML), 5 ML MULTIDOSE VIAL COMPOUNDED.  Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272",
      "product_quantity": "8 vials",
      "reason_for_recall": "Lack of assurance of sterility for injectables and solutions intended to be sterile.",
      "recall_initiation_date": "20190408",
      "center_classification_date": "20190430",
      "termination_date": "20230519",
      "report_date": "20190508",
      "code_info": "Lot #: 01232019@25, Exp 4/23/19"
    }
  ]
}