{
  "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": "Princeton",
      "address_1": "100 College Rd W",
      "reason_for_recall": "Subpotent Drug: out of specification results for assay test.",
      "address_2": "",
      "product_quantity": "a) 10,200 bottles; b) 300 bottles",
      "code_info": "Lot #: a) FJ6599, Exp 05/17 and b) FJ6600, Exp 05/17",
      "center_classification_date": "20170119",
      "distribution_pattern": "Nationwide in the USA",
      "state": "NJ",
      "product_description": "Donepezil Hydrochloride Tablets, 10 mg, packaged in a) 30-count bottles (NDC 0781-5275-31) and b) 1000-count bottles (NDC 0781-5275-10), Rx only, Manufactured in India by Sandoz Private Ltd for Sandoz Inc., Princeton, NJ 08540.",
      "report_date": "20170125",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Sandoz Inc",
      "recall_number": "D-0435-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "75987",
      "termination_date": "20170914",
      "more_code_info": "",
      "recall_initiation_date": "20161213",
      "postal_code": "08540-6604",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}