{
  "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": "Labeling: Incorrect or Missing Lot and/or Exp Date: Greenstone LLC is recalling  Nifedipine Extended Release tablets (90mg). The expiration date on the package is 48 months instead of 36 months.",
      "address_2": "",
      "product_quantity": "21600 tablets",
      "code_info": "V110079",
      "center_classification_date": "20140116",
      "distribution_pattern": "Nationwide",
      "state": "NJ",
      "product_description": "Nifedipine, extended-release tablets, 90mg 100 count blister pack,  Rx only, Distributed by: GREENSTONE LLC, Pespack, NJ,07977, NDC 59762-6692-8",
      "report_date": "20140122",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Greenstone Llc",
      "recall_number": "D-737-2014",
      "initial_firm_notification": "Telephone",
      "product_type": "Drugs",
      "event_id": "66760",
      "termination_date": "20150605",
      "more_code_info": "",
      "recall_initiation_date": "20131101",
      "postal_code": "07977",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}