{
  "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": "Marketed without an Approved NDA/ANDA: This recall is being initiated because of changes to the dissolution profile in distributed lots resulting from a manufacturing site change. There is currently no approved application supporting the alternate manufacturing site.",
      "address_2": "",
      "product_quantity": "2796 bottles",
      "code_info": "Lot #:  V121207, V121208, Exp 03/31/2017",
      "center_classification_date": "20131120",
      "distribution_pattern": "Nationwide and Puerto Rico",
      "state": "NJ",
      "product_description": "Spironolactone tablets, USP 25 mg, Rx only, 500 count bottle, Distributed By: Greenstone LLC, Peapack, NJ 07977, NDC: 59762-5011-2.",
      "report_date": "20131127",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Greenstone Llc",
      "recall_number": "D-010-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "66822",
      "termination_date": "20170413",
      "more_code_info": "",
      "recall_initiation_date": "20130904",
      "postal_code": "07977",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}