{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "South Plainfield",
      "state": "NJ",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "80878",
      "recalling_firm": "ACP Nimble Buyer, Inc.",
      "address_1": "111 Coolidge St",
      "address_2": "",
      "postal_code": "07080-3801",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide within the United States",
      "recall_number": "D-0514-2019",
      "product_description": "Mometasone Furoate Cream, 0.1%, 45 g tube, Rx Only, Manufactured by: G&W Laboratories, Inc. South Plainfield, NJ 07080, NDC 0713-0726-37",
      "product_quantity": "58,176 units",
      "reason_for_recall": "Labeling: Not Elsewhere Classified. Mometasone Furoate Cream has an NDC typographical error.",
      "recall_initiation_date": "20190207",
      "center_classification_date": "20190220",
      "termination_date": "20200323",
      "report_date": "20190227",
      "code_info": "Lot #: 1009431, 1009507, Exp. 08/2020; 1009886, Exp. 09/2020",
      "more_code_info": ""
    }
  ]
}