{
  "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-1274-2017",
      "product_description": "Bayview Breast Pack, part number 009080-2",
      "product_quantity": "126 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    84687, 2/24/2018  86231, 2/9/2018  89386, 4/8/2018  94891, 4/23/2018  95261, 4/12/2018  95968, 4/1/2018  96742, 4/23/2018",
      "more_code_info": ""
    }
  ]
}