{
  "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,
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "New York",
      "state": "NY",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "82452",
      "recalling_firm": "Estee Lauder Inc",
      "address_1": "767 5th Ave Fl 47th",
      "address_2": "N/A",
      "postal_code": "10153-0023",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.A. Nationwide",
      "recall_number": "D-1132-2019",
      "product_description": "Repairwear Laser Focus Line Smoothing Cream Broad Spectrum SPF 15, packaged in a light green folding carton containing a 50 mL silver jar with a silver cap, Clinique Laboratories, Dist. New York, NY 10022",
      "product_quantity": "14490 jars",
      "reason_for_recall": "Defective container: Ineffective seal between the cap and jar of the affected product.",
      "recall_initiation_date": "20190315",
      "center_classification_date": "20190415",
      "termination_date": "20250113",
      "report_date": "20190424",
      "code_info": "Lot #: A68"
    }
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}