{
  "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": "2026-09-17",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "215148",
      "product_res_number": "Z-2484-2025",
      "event_date_initiated": "2025-08-06",
      "event_date_posted": "2025-09-05",
      "recall_status": "Open, Classified",
      "res_event_number": "97303",
      "product_code": "KTI",
      "k_numbers": [
        "K193517"
      ],
      "product_description": "ViziShot 2FLEX. Single Use Aspiration Needle. Model Number: NA-U403SX-4019.\n\nThe ViziShot 2 FLEX tissue biopsy device is made up of four main parts: a handle, a sheath, a needle, and a stylet. The sheath and needle are attached to the handle, and the stylet, which is removable, is located inside the needle tube.",
      "code_info": "Model Number: NA-U403SX-4019. UDI-DI: 00821925043060.         \n\nLot numbers: All lots manufactured after 7/29/2022.",
      "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": "Potential for undetected, deformed a-traumatic tips.",
      "root_cause_description": "Process design",
      "action": "Olympus notified consignees on about 08/06/2025 via letter. Consignees were instructed to examine inventory and quarantine any affected units, ensure all users of the device carefully read the content of this notification, including the reinforced text from the IFU and the product removal information, arrange for the return of affected units, and acknowledge receipt of the recall notification via the Olympus web portal. Consignees were also instructed to notify customers if the affected units were further distributed.\n***Update 12/31/2025*** URGENT MEDICAL DEVICE RECALL letters were sent to additional customers on January 9, 2026 with identical instructions. ***Edit 3/23/26: January 9, 2026 letters users were instructed to return all affected devices.",
      "product_quantity": "104,508 units",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Australia, Germany, Canada, Chile, China, Hong Kong, India, Japan, Singapore.",
      "openfda": {
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        "device_name": "Bronchoscope Accessory",
        "medical_specialty_description": "Ear, Nose, Throat",
        "regulation_number": "874.4680",
        "device_class": "2"
      }
    }
  ]
}