{
  "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": "2026-07-29",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "status": "Terminated",
      "city": "Visalia",
      "state": "CA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "88409",
      "recalling_firm": "Je Dois Lavoir LLC",
      "address_1": "3936 E Evergreen Ave",
      "address_2": "N/A",
      "postal_code": "93292-1281",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Sold online via website nationwide in the USA and Canada.",
      "recall_number": "D-0631-2022",
      "product_description": "365 SKINNY High Intensity Capsules, 600 mg,  30-count bottle, BODY BALANCE INTERNACIONAL",
      "product_quantity": "783 bottles",
      "reason_for_recall": "Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared sibutramine, a previously approved drug that was withdrawn from the US market due to safety concerns.",
      "recall_initiation_date": "20210802",
      "center_classification_date": "20220223",
      "termination_date": "20230502",
      "report_date": "20220223",
      "code_info": "Lot 102-26, Exp Dec 2022"
    }
  ]
}