{
  "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,
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  "results": [
    {
      "status": "Terminated",
      "city": "Saint Louis",
      "state": "MO",
      "country": "United States",
      "classification": "Class I",
      "openfda": {
        "application_number": [
          "NDA022572"
        ],
        "brand_name": [
          "MITOSOL"
        ],
        "generic_name": [
          "MITOMYCIN"
        ],
        "manufacturer_name": [
          "Mobius Therapeutics LLC"
        ],
        "product_ndc": [
          "49771-002"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "rxcui": [
          "1244553",
          "1244558"
        ],
        "spl_id": [
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        "spl_set_id": [
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        "package_ndc": [
          "49771-002-01",
          "49771-002-03"
        ],
        "is_original_packager": [
          true
        ]
      },
      "product_type": "Drugs",
      "event_id": "64018",
      "recalling_firm": "Mobius Therapeutics LLC",
      "address_1": "4041 Forest Park Ave",
      "address_2": "N/A",
      "postal_code": "63108-3213",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Nationwide and Military and Government Consignees",
      "recall_number": "D-809-2013",
      "product_description": "Mitosol (mitomycin for solution), 0.2 mg/vial, Kit for Ophthalmic Use (NDC 49771-002-01), 3 kits per box (NDC 49771-002-03), Rx only, Manufactured for: Mobius Therapeutics, LLC, 4041 Forest Park Avenue, St. Louis, MO  63108 USA.",
      "product_quantity": "83 boxes",
      "reason_for_recall": "Non-Sterility: one or more components of the kit have been found to be contaminated with yeast.",
      "recall_initiation_date": "20130103",
      "center_classification_date": "20130719",
      "termination_date": "20130729",
      "report_date": "20130731",
      "code_info": "Lot #: M086920 and M098260, Exp. 08/2013",
      "more_code_info": ""
    }
  ]
}