{
  "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": "78366",
      "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": "E-Mail",
      "distribution_pattern": "US Distribution to the state of : SC",
      "recall_number": "Z-0069-2018",
      "product_description": "AMS, ALIGNED MEDICAL SOLUTIONS, T&A Pack, AMS6357, STERILE EO.",
      "product_quantity": "60 kits",
      "reason_for_recall": "Custom surgical kits were manufactured with part #63310 Catheter Urethral 10FR 16\" which were subsequently recalled by CR Bard for a potential sterile barrier breach.",
      "recall_initiation_date": "20171024",
      "center_classification_date": "20171107",
      "termination_date": "20180702",
      "report_date": "20171115",
      "code_info": "Lot # 109138"
    }
  ]
}