{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Irvine",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95426",
      "recalling_firm": "Nihon Kohden America Inc",
      "address_1": "15353 Barranca Pkwy",
      "address_2": "N/A",
      "postal_code": "92618-2216",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, KS, MA, MD, MI, MO, MT, NC, ND, NE, NH, OK, PA, SC, TX, VT, WA, and WI.  O.U.S.: N/A",
      "recall_number": "Z-0268-2025",
      "product_description": "Nihon Kohden Adult Ear Clip SpO2 Sensor, 1.5 meter Model 809030007    Reusable SpO2 Ear Clip, each",
      "product_quantity": "64",
      "reason_for_recall": "Due to oximeters not having FDA market approval or clearance to distribute in the U.S.",
      "recall_initiation_date": "20240918",
      "center_classification_date": "20241030",
      "report_date": "20241106",
      "code_info": "Model num.: 809030007 UDI-DI: 06970758500159 All lot numbers",
      "more_code_info": ""
    }
  ]
}