{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Orlando",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66191",
      "recalling_firm": "Pinook-Usa",
      "address_1": "901 Central Florida Pkwy Ste A6",
      "address_2": "N/A",
      "postal_code": "32824-8508",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) including  Puerto Rico and Guam and the states of AZ, CA, CO, FL, IL, MA, MD, MO, MT, NC, ND, NJ, NV, NY, TX, VA, and WA and the country of Canada.",
      "recall_number": "Z-0176-2014",
      "product_description": "Pinook Mini Massager   Distributed by www.pinookusa.com.    Used to strengthen the abdominal muscles.",
      "product_quantity": "28,994 units (Mini and Micro)",
      "reason_for_recall": "Failure to submit a premarket submission and gain approval of a medical device.",
      "recall_initiation_date": "20130523",
      "center_classification_date": "20131107",
      "termination_date": "20160929",
      "report_date": "20131113",
      "code_info": "ALL LOTS"
    }
  ]
}