{
  "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": "Beverly Hills",
      "state": "CA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "66897",
      "recalling_firm": "Tendex",
      "address_1": "311 Robertson Blvd",
      "address_2": "Suite 454",
      "postal_code": "90211",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Nationwide.",
      "recall_number": "D-1346-2014",
      "product_description": "NATURECT Capsules Dietary Supplement 500 mg, supplied in 1 count blister pack and 5, 10, 20, and 40- count bottles, Distributed by P-Boost, Los Angeles, CA 900466",
      "product_quantity": "unknown",
      "reason_for_recall": "Marketed Without an Approved NDA/ANDA: FDA analysis found the product to contain undeclared active ingredient, tadalafil, thus making these products unapproved drugs.",
      "recall_initiation_date": "20131119",
      "center_classification_date": "20140521",
      "termination_date": "20140918",
      "report_date": "20140528",
      "code_info": "Lot # F51Q.  EXP: 07/16    The UPC Codes for Naturect are:   1ct- 893020242013  5ct - 893020242051  10ct - 893020242105  20ct - 893020242204  40ct - 893020242402"
    }
  ]
}