{
  "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": "Tokyo",
      "state": "N/A",
      "country": "Japan",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75511",
      "recalling_firm": "Lsi Medience Corporation",
      "address_1": "13-4 Uchikanda 1 Chome",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Distribution to the states of : AL, FL, ID and MA.",
      "recall_number": "Z-0646-2017",
      "product_description": "Pathfast D-Dimer, Reference number: PF1051-KUS",
      "product_quantity": "42 boxes (each containing 60 test cartridges/one kit contains 10 reagent cartridge trays and one tray has 6 cartridges).",
      "reason_for_recall": "Two complaints were received about decrease in sensitivity (control value and/or calibration value) of the product.",
      "recall_initiation_date": "20160816",
      "center_classification_date": "20161121",
      "termination_date": "20170227",
      "report_date": "20161130",
      "code_info": "Lot T528"
    }
  ]
}