{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Nobeoka-shi",
      "state": "",
      "country": "Japan",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63146",
      "recalling_firm": "Asahi Kasei Medical Co., Ltd., Okatomi Plant",
      "address_1": "4960 5 Chome Nakagawara Cho",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "REXEED SX:  Worldwide Distribution - USA including TN and the countries of Japan and Germany    REXEED LX:    Worldwide Distribution - USA including TN and Germany",
      "recall_number": "Z-2423-2012",
      "product_description": "Asahi KASEI, REXEED(TM)- 15 LX, HEMODIALYZER    dialysis filter",
      "product_quantity": "24 units",
      "reason_for_recall": "Asahi became aware of a negative trend for rate of the adverse events that may be associated with a manufacturing change to certain lot numbers of the products, though there is no sufficient information to date to conclusively link these adverse events to the products.",
      "recall_initiation_date": "20120921",
      "center_classification_date": "20120920",
      "termination_date": "20130205",
      "report_date": "20120926",
      "code_info": "Lot number:  296T78",
      "more_code_info": ""
    }
  ]
}