{
  "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": "76280",
      "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": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Distributed in AZ, CA, CO, CT, FL, GA, IL, IN, KS, LA, MA, MD, MI, MN, MO, NC, ND, NE, NJ, NV, OH, PA, TX, UT, VA, and WA.",
      "recall_number": "Z-1286-2017",
      "product_description": "Custom Venous Kit, part number TVS4024(C",
      "product_quantity": "544 kits",
      "reason_for_recall": "The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits were recalled because gloves may contain splits or holes compromising sterility.",
      "recall_initiation_date": "20170111",
      "center_classification_date": "20170228",
      "termination_date": "20170503",
      "report_date": "20170308",
      "code_info": "Lot number and expiration date    84766, 1/8/2018  85230, 1/12/2018  85938, 1/7/2018  88327, 1/6/2018  88591, 1/9/2018  96129, 1/11/2018  96256, 1/1/2018  96660, 1/2/2018  98425, 1/24/2018",
      "more_code_info": ""
    }
  ]
}