{
  "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-0240-2017",
      "product_description": "Minor Lithotomy Pack, Kit number 002650-7    convenience custom kits used for general surgery in hospital operating room",
      "product_quantity": "114 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:    66523 1/31/2014  61660 2/2/2014  61505 2/24/2014  60540 3/30/2014  67197 9/10/2014  65055 9/30/2014  58208 7/5/2016  68949 9/12/2016  71055 12/27/2016"
    }
  ]
}