{
  "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": [
    {
      "country": "United States",
      "city": "Queen Creek",
      "address_1": "530 E Hunt Hwy",
      "reason_for_recall": "Marketed Without an Approved NDA/ANDA; products have been found to contain tadalafil, the active ingredient in an FDA approved product used to treat erectile dysfunction, making this product an unapproved drug",
      "address_2": "Ste 103",
      "product_quantity": "145,632 capsules",
      "code_info": "All lots of product distributed and sold from January 2012 to May 7, 2013.    SKUs: SKUs 626570613855, 626570619055, 626570617860, 626570617563",
      "center_classification_date": "20130905",
      "distribution_pattern": "US states nationwide and international.",
      "state": "AZ",
      "product_description": "Velextra All-Natural Herbal Supplement, packaged in 1 & 2 capsule blister packs and 4, 10 & 12 capsule bottles, Manufactured For: BeaMonstar Products Queen Creek, AZ",
      "report_date": "20130911",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Beamonstar Products",
      "recall_number": "D-930-2013",
      "initial_firm_notification": "E-Mail",
      "product_type": "Drugs",
      "event_id": "65130",
      "termination_date": "20140421",
      "more_code_info": "",
      "recall_initiation_date": "20130501",
      "postal_code": "85243",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}