{
  "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": "2026-07-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Largo",
      "state": "FL",
      "country": "United States",
      "classification": "Class III",
      "openfda": {
        "application_number": [
          "ANDA210370"
        ],
        "brand_name": [
          "MYCOPHENOLATE MOFETIL"
        ],
        "generic_name": [
          "MYCOPHENOLATE MOFETIL"
        ],
        "manufacturer_name": [
          "VistaPharm, LLC"
        ],
        "product_ndc": [
          "66689-307"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "ORAL"
        ],
        "substance_name": [
          "MYCOPHENOLATE MOFETIL"
        ],
        "rxcui": [
          "311880"
        ],
        "spl_id": [
          "ae50c781-e225-4275-a23a-03b4b2a1e507"
        ],
        "spl_set_id": [
          "175d8b87-e06a-4c9e-b3de-378114b52274"
        ],
        "package_ndc": [
          "66689-307-08"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "9242ECW6R0"
        ]
      },
      "product_type": "Drugs",
      "event_id": "93322",
      "recalling_firm": "VistaPharm LLC",
      "address_1": "7265 Ulmerton Rd",
      "address_2": "",
      "postal_code": "33771-4809",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide and Saudi Arabia",
      "recall_number": "D-0093-2024",
      "product_description": "Mycophenolate Mofetil for Oral Suspension, USP, 200 mg/mL, Rx Only, bottle, Manufactured for: VistaPharm, Inc., Largo, FL 33771, USA, NDC#66689-307-08.",
      "product_quantity": "11,633 bottles",
      "reason_for_recall": "Defective Container: The adaptor does not fit into the neck of the bottle after reconstitution with water.",
      "recall_initiation_date": "20231026",
      "center_classification_date": "20231108",
      "termination_date": "20250321",
      "report_date": "20231115",
      "code_info": "Lot #: M23400A, M23401A, M23402A, Exp Date. 04/30/2025; M23591A, M23592A, Exp Date. 06/30/2025.",
      "more_code_info": ""
    }
  ]
}