{
  "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": [
    {
      "status": "Terminated",
      "city": "Princeton",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "76435",
      "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 in the USA and Puerto Rico",
      "recall_number": "D-0481-2017",
      "product_description": "Transderm Scop (scopolamine) Transdermal System, 1.5 mg, 1 patch per pouch (NDC 66758-208-58), packaged in 4-count patches per carton (NDC 66758-208-54), Rx Only, Manufactured by ALZA Corporation, Vacaville, CA  95688 for Sandoz Inc., Princeton, NJ  08540.",
      "product_quantity": "157,922 cartons",
      "reason_for_recall": "Labeling: Incorrect Instructions:outer carton contains the incorrect instructions for Step 2 stating \"Do cut the patch\" rather than the correct instructions of \"Do not cut the patch\". The pouch containing the patch is labeled correctly.",
      "recall_initiation_date": "20170202",
      "center_classification_date": "20170217",
      "termination_date": "20171024",
      "report_date": "20170301",
      "code_info": "Lot #: 6323Q11, 6328Q11, Exp 06/19; 6355Q11, Exp 07/19"
    }
  ]
}