{
  "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": "South San Francisco",
      "address_1": "1 DNA Way",
      "reason_for_recall": "Short Fill: some bottles contained less than 120-count per labeled claim.",
      "address_2": "",
      "product_quantity": "1128 bottles",
      "code_info": "Lot #: a) M1365B01, Exp 04/15; b) M1365, Exp 04/15",
      "center_classification_date": "20121220",
      "distribution_pattern": "Nationwide",
      "state": "CA",
      "product_description": "CellCept (mycophenolate mofetil) capsules, 250 mg, packaged in a) 12 x 120-count bottles per carton, NDC 0004-0259-05; b) 120-count capsules per bottle, NDC 0004-0259-51; Made in Ireland; Distributed by: Genentech USA, Inc., South San Francisco, CA  94080.",
      "report_date": "20121226",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Genentech, Inc.",
      "recall_number": "D-097-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "63874",
      "termination_date": "20141120",
      "more_code_info": "",
      "recall_initiation_date": "20120927",
      "postal_code": "94080-4990",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}