{
  "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-0250-2017",
      "product_description": "OB/GYN Pack, Kit number AMS2038    convenience custom kits used for general surgery in hospital operating room",
      "product_quantity": "18 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 Number/ Expiration Date:  58648 4/17/2015"
    }
  ]
}