{
  "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": "2026-08-27",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "216278",
      "product_res_number": "Z-0452-2026",
      "event_date_initiated": "2025-10-08",
      "event_date_posted": "2025-11-07",
      "recall_status": "Open, Classified",
      "res_event_number": "97665",
      "product_code": "FEO",
      "k_numbers": [
        "K171024"
      ],
      "product_description": "Brand Name: Lithotriptor, Ultrasonic\nProduct Name: ShockPulse Lithotripsy Transducer\nModel/Catalog Number: SPL-T\nProduct Description: The ShockPulse Lithotripsy System is an electromechanical device capable of fragmenting calculi and aspirating stone debris. The ShockPulse transducer is a reusable device that requires cleaning and steam sterilization prior to use in order to generate both low-frequency mechanical impacts and high-frequency ultrasonic energy that quickly disintegrates stones.\nComponent: ShockPulse Lithotripsy System",
      "code_info": "Model/Catalog Number: SPL-T;\nUDI-PI: 00855279005023;\nAll serial numbers;",
      "firm_fei_number": "2429304",
      "recalling_firm": "Olympus Corporation of the Americas",
      "address_1": "3500 Corporate Pkwy",
      "city": "Center Valley",
      "state": "PA",
      "postal_code": "18034-8229",
      "additional_info_contact": "Cynthia Ow\n647-9993203",
      "reason_for_recall": "The device may either fail to start up, or the transducer may start briefly and then stop, accompanied by an error light on the generator. In addition, the body of the transducer handpiece may gradually increase in temperature during clinical use.",
      "root_cause_description": "Device Design",
      "action": "On October 8, 2025 URGENT: MEDICAL DEVICE ADVISORY NOTICE letters were sent to customers. Actions to be taken: Ensure you read the content of the notice. Ensure that all personnel are aware and knowledgeable on the content of the notice. You may continue to use the device according to the instruction for use, which cautions users to ensure that a back-up transducer and probe are sterilized and available prior to beginning a procedure. If you have further distributed this product, identify your customers, and forward them this notification. Olympus requests that you acknowledge receipt of this letter with the provided reply form.",
      "product_quantity": "1528 units",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Canada, India, Taiwan, Germany, Australia, Singapore.",
      "openfda": {
        "k_number": [
          "K973251",
          "K842024",
          "K873367",
          "K182490",
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          "K181997",
          "K230893",
          "K171024",
          "K850298",
          "K993046",
          "K173234",
          "K181364",
          "K142428"
        ],
        "device_name": "Lithotriptor, Ultrasonic",
        "medical_specialty_description": "Gastroenterology, Urology",
        "regulation_number": "876.4480",
        "device_class": "2",
        "registration_number": [
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        "fei_number": [
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}