{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "196577",
      "product_res_number": "Z-0244-2023",
      "event_date_initiated": "2022-10-14",
      "event_date_posted": "2022-11-17",
      "recall_status": "Open, Classified",
      "res_event_number": "91041",
      "product_code": "ONO",
      "k_numbers": [
        "K053087",
        "K181859",
        "K211269"
      ],
      "product_description": "Visualase Cooled Laser Applicator System (VCLAS) 9735560 .4MM CORE\nFIBER 10MM TIP product.  Used to necrotize or coagulate soft tissue by physicians in minimally invasive surgical procedures.",
      "code_info": "Product Number/CFN: 9735560\nUDI-DI Code: 00763000416430\nLot Numbers:\n0224382403, 0224779378, 0224824522, 0224824523, 0224824525,\n0224824767, 0224824768, 0224824769",
      "firm_fei_number": "1000517638",
      "recalling_firm": "Medtronic Navigation, Inc.",
      "address_1": "826 Coal Creek Cir",
      "city": "Louisville",
      "state": "CO",
      "postal_code": "80027-9710",
      "additional_info_contact": "Naomi Rodiles\n612-427-5521",
      "reason_for_recall": "Due to a defect in the outer pouch sterile seal",
      "root_cause_description": "Nonconforming Material/Component",
      "action": "On 10/03/2022, the firm verbally notified affected customers and on 10/14/2022 sent an \"URGENT: MEDICAL DEVICE CORRECTION\" Letter to customer informing them that Medtronic identified a breach to the sterile barrier of the outer pouch of specific lots of VCLAS 9735560 .4MM Core Fiber 10MM Tip products.\n\nCustomer are instructed to:\nimmediately identify and segregate affected products within your inventory. Medtronic will contact you to facilitate product replacement when unaffected product is available.\n\nMedtronic has determined that the inner pouches maintain sterility, accordingly, you may use segregated products ensuring the following sterile technique workflow is followed:\n1. Open the affected outer pouch outside of the sterile field and remove the smaller internal pouches.\n2. Per the Instruction for Use: Prior to use, examine the product packaging (in this instance the inner pouch) for damage, deterioration, and expired shelf life. If found, do not use the product.\n3. Open the internal pouches using sterile technique and carefully transfer the sterile contents into the sterile field.\n\nFor questions, contact Medtronic Technical Service at 1-888-826-5603 or email at rs.navtechsupport@medtronic.com",
      "product_quantity": "95 units",
      "distribution_pattern": "U.S. Nationwide distribution including in the states AZ, CA, CO, DC, FL, IL, KY, MA, MD, ME, MI, MN, MO, NH, NJ, NY, OH, PA, RI, TX, VA, WA, and WV.",
      "openfda": {
        "k_number": [
          "K211269",
          "K214125",
          "K251298",
          "K260976",
          "K240877",
          "K253391",
          "K250307"
        ],
        "registration_number": [
          "2183744",
          "1045254",
          "1723170",
          "3012452798",
          "3009970070",
          "3018094310",
          "3006849754"
        ],
        "fei_number": [
          "2183744",
          "1045254",
          "1000517638",
          "3012452798",
          "3009970070",
          "3018094310",
          "3006849754"
        ],
        "device_name": "Neurosurgical Laser With Mr Thermography",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4810",
        "device_class": "2"
      }
    }
  ]
}