{
  "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": "Peapack",
      "address_1": "100 Route 206 North",
      "reason_for_recall": "Failed Dissolution Specification; the bulk lot yielded an out of specification result at the 8 hr timepoint, 18 month interval",
      "address_2": "",
      "product_quantity": "22,529 bottles",
      "code_info": "lot V112000, EXP Jun 2016",
      "center_classification_date": "20140203",
      "distribution_pattern": "US Nationwide (including PR)",
      "state": "NJ",
      "product_description": "Glipizide XL (glipizide) extended release tablets, 5 mg , 500 count bottles, Rx only, Distributed by: Greenstone Ltd., Peapack, NJ ---  NDC 59762-5032-2",
      "report_date": "20140212",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Greenstone Llc",
      "recall_number": "D-1059-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "66814",
      "termination_date": "20150624",
      "more_code_info": "",
      "recall_initiation_date": "20131104",
      "postal_code": "07977",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}