{
  "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-0220-2017",
      "product_description": "Laparoscopy Pack, Kit number AMS2537 and AMS2537(A    convenience custom kits used for general surgery in hospital operating room",
      "product_quantity": "184 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:    62091 11/7/2015  62893 1/22/2016  64647 7/14/2016  69438 9/16/2016  69184 9/25/2016  70969 10/20/2016  72483 1/17/2017  73353 3/12/2017"
    }
  ]
}