{
  "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,
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  "results": [
    {
      "status": "Terminated",
      "city": "Williamstown",
      "state": "NJ",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "66406",
      "recalling_firm": "Haute Health, LLC",
      "address_1": "614 Atlanta Ct",
      "address_2": "N/A",
      "postal_code": "08094-3549",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Nationwide and internationally via internet sales.",
      "recall_number": "D-1235-2014",
      "product_description": "Prolifta Dietary Supplement Prolifta, 400mg/capsule, Packaged in 1 and 2 capsule blister packs and 4, 12, and 24 capsule bottles   Made in the USA Distributed by: Prolifta LLC 1+877.239.8231  www.proliftaherbal.com.",
      "product_quantity": "172,800 capsules",
      "reason_for_recall": "Marketed without an Approved NDA/ANDA: Dietary supplement may contain amounts of an active ingredient found in some FDA-approved drugs for erectile dysfunction (ED) making the dietary supplement an unapproved drug.",
      "recall_initiation_date": "20130927",
      "center_classification_date": "20140415",
      "termination_date": "20150129",
      "report_date": "20140423",
      "code_info": "All lot codes and expiration dates."
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}