{
  "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": "Nixa",
      "state": "MO",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "67228",
      "recalling_firm": "Schindele Enterprises dba Midwest Wholesale",
      "address_1": "617 N Althea Ave",
      "address_2": "N/A",
      "postal_code": "65714-7432",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Distributed to PA, IL, TX, IA, GA, CT, FL, CA, LA, NY, MD, NV, and WI",
      "recall_number": "D-1337-2014",
      "product_description": "MiracleZEN Platinum, 1 pill blister pack, 2000 mg capsule, Distributed by: Power Life Distributors, COK Inc., Los Angeles, CA.",
      "product_quantity": "49 blister packs",
      "reason_for_recall": "Marketed Without an Approved NDA/ANDA: These dietary supplements contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.",
      "recall_initiation_date": "20140109",
      "center_classification_date": "20140520",
      "termination_date": "20150203",
      "report_date": "20140528",
      "code_info": "1 pill blister packs: Lot  OAWF 1027 Exp 1/31/2015 and  Lot OAWF1003 Exp 01/31/2015."
    }
  ]
}