{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Billings",
      "state": "MT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71968",
      "recalling_firm": "Windstone Medical Packaging, Inc.",
      "address_1": "1602 4th Ave N",
      "address_2": "N/A",
      "postal_code": "59101-1521",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution to California, Florida, Georgia, Illinois, Kansas, Louisiana, Michigan, New Jersey, Nevada, Texas, Virginia, and Wyoming.",
      "recall_number": "Z-0151-2017",
      "product_description": "Bayview Abdominoplasty Pack, Kit part number 009079-1  convenience custom kits used for general surgery in hospital operating room",
      "product_quantity": "90 kits",
      "reason_for_recall": "The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the custom AMS kit were recalled because gloves may contain splits or holes compromising sterility.",
      "recall_initiation_date": "20150422",
      "center_classification_date": "20161020",
      "termination_date": "20161025",
      "report_date": "20161026",
      "code_info": "Lot Numbers/Expiration Dates:    57718 6/18/2016  60804 5/16/2015  62210 5/7/2015  62802 6/6/2015  66875 11/20/2015  72825 7/29/2016  73912 7/5/2016"
    }
  ]
}