{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "26592",
      "product_res_number": "Z-0769-03",
      "event_date_initiated": "2003-03-25",
      "event_date_posted": "2003-04-22",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-09-09",
      "res_event_number": "25830",
      "product_description": "BAND BAG",
      "code_info": "Catalog Number CPA-50025 Lot Numbers 007253627, 007253628, 007253629, 007253630, 007253631, 007253632, 007253633, 007253634.",
      "firm_fei_number": "1000125955",
      "recalling_firm": "Windstone Medical, Inc.",
      "address_1": "1602 4th Ave North",
      "city": "Billings",
      "state": "MT",
      "postal_code": "59101",
      "additional_info_contact": "Troy Berquist\n406-259-6387",
      "reason_for_recall": "Product contains latex, but not labeled as containing latex.",
      "root_cause_description": "Other",
      "action": "On 3/25/03 the firm contacted their customers by telephone.  This was followed by a letter dated 3/25/03.  Enclosed with the letter is a response form for the customer to fill out and return to the firm.  Product is to be returned to the firm.",
      "product_quantity": "200",
      "distribution_pattern": "The firm distributed to 13 hospitals and medical facilities located in CO,  IN, MI,  MN,  MT, UT, and WA.",
      "openfda": {}
    }
  ]
}