{
  "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": "Amityville",
      "state": "NY",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "65803",
      "recalling_firm": "Hi-Tech Pharmacal Co., Inc.",
      "address_1": "369 Bayview Ave",
      "address_2": "",
      "postal_code": "11701-2801",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide and Puerto Rico",
      "recall_number": "D-888-2013",
      "product_description": "Clobetasol Propionate Cream, USP, 0.05%, 15 grams, Rx only, Hi-Tech PHARMACAL label, Hi-Tech Pharmacal, Co., Inc., Amityville, NY 11701, NDC 50383-267-15 --- For dermatologic use only.  Product is packaged into tubes and then placed into unit cartons.",
      "product_quantity": "58,812 tubes",
      "reason_for_recall": "Labeling: Label Mix-up; some cartons labeled as Clobetasol Propionate Cream USP contain tubes labeled as Clobetasol Propionate Gel USP.  The actual product in the tube is Clobetasol Propionate Cream USP",
      "recall_initiation_date": "20130725",
      "center_classification_date": "20130813",
      "termination_date": "20160516",
      "report_date": "20130821",
      "code_info": "Batch/Lot 619442, exp. 01/2015",
      "more_code_info": ""
    }
  ]
}