{
  "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": "South San Francisco",
      "state": "CA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "79175",
      "recalling_firm": "Genentech, Inc.",
      "address_1": "1 Dna Way",
      "address_2": "",
      "postal_code": "94080-4990",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed throughout the United States",
      "recall_number": "D-0416-2018",
      "product_description": "Klonopin (clonazepam) 0.5 mg Tablets,100-count bottle, Rx only. Made in Canada, Distributed by Genentech USA, Inc. A Member of the Roach Group, 1 DNA Way South San Francisco, CA 94080-4990. NDC 0004-0068-01",
      "product_quantity": "3,192 bottles",
      "reason_for_recall": "Labeling: Not Elsewhere Classified: Schedule IV controlled substance indicator of CIV being omitted  from the product carton, primary label is correct.",
      "recall_initiation_date": "20180205",
      "center_classification_date": "20180213",
      "termination_date": "20180906",
      "report_date": "20180221",
      "code_info": "Lot # 3141989, EXP 08/31/2019",
      "more_code_info": ""
    }
  ]
}