{
  "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": "Princeton",
      "state": "NJ",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "73035",
      "recalling_firm": "Sandoz Inc",
      "address_1": "100 College Rd W",
      "address_2": "N/A",
      "postal_code": "08540-6604",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0659-2016",
      "product_description": "Candesartan Cilexetil Tablets, 16 mg, a) 30 count (NDC 00781-5938-31) and b) 90 count (NDC 00781-5938-92) bottles, Rx Only, Manufactured by Mylan Laboratories Limited Hyderabad 500 034, India for Sandoz Inc. Princeton, NJ 08540",
      "product_quantity": "277,267 bottles",
      "reason_for_recall": "Failed Impurities/Degradation Specifications; 9 month stability timepoint",
      "recall_initiation_date": "20151231",
      "center_classification_date": "20160211",
      "termination_date": "20170412",
      "report_date": "20160217",
      "code_info": "a)   3022288 12/2015  3025988 03/2016  3025989 04/2016  3030459 08/2016  3030460 08/2016  3032087 10/2016  3032088 10/2016  3034506 12/2016  3035952 01/2017  3035953 01/2017    b)   3022287 12/2015  3025990 04/2016  3030458 08/2016  3032086 09/2016  3035954 01/2017",
      "more_code_info": ""
    }
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}