{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "202960",
      "product_res_number": "Z-0155-2024",
      "event_date_initiated": "2023-08-17",
      "event_date_posted": "2023-10-24",
      "recall_status": "Open, Classified",
      "res_event_number": "92943",
      "product_code": "OBH",
      "k_numbers": [
        "K180126"
      ],
      "product_description": "SOZO Bilateral Arm L-Dex Software",
      "code_info": "UDI-DI: B277SFT0250.\n\nSoftware v4.1 and v5.0",
      "firm_fei_number": "3004782476",
      "recalling_firm": "Impedimed Limited",
      "address_1": "50 building parker ct",
      "address_2": "U 1",
      "city": "Pinkenba",
      "country": "Australia",
      "additional_info_contact": "61 7 34231777",
      "reason_for_recall": "Bilateral L-Dex assessment software does not have the same level of sensitivity to help detect early signs of lymphedema as the unilateral arm L-Dex assessment, which could result in under-recognition of early lymphedema, which could result in delay in early intervention, and more aggressive intervention.",
      "root_cause_description": "Device Design",
      "action": "On 8/17/23, correction notices were emailed to customers.  Customers were asked to take the following actions:\n\nWe recommend that you confirm the risk profile of your bilateral arm patients in MySOZO and take the following actions:\n- For patients at unilateral risk for lymphedema (over 90% of breast cancer patients), confirm that the unilateral arm L-Dex assessment is selected in the patient profile and continue to screen for early signs of lymphedema.\n- For patients at bilateral risk for lymphedema (3-10% of breast cancer patients), guidelines suggest routine screening using clinical exam and symptom assessment.\n- Complete and return the response form via link: https://forms.office.com/r/kafiuDbw21\n\nIn September, the firm will be issuing a SOZO software update to make unilateral L-Dex the sole assessment option for arms. L-Dex assessments for legs will not be impacted.\n\nThis correction letter should be shared with anyone within your organization who needs to be aware of the correction or with any organization where the device may have been transferred.\n\nIf you have questions or need to report quality issues, call 1/877/247-0111, Option 4 (Mon-Fri, 8:00 am - 8:00 om ET) or email impedimed156@impedimed.com",
      "product_quantity": "354",
      "distribution_pattern": "US Nationwide distribution in the states of IA, CA, IL, AK, NY, FL, KS, WI, MI, NC, GA, SD, KY, TX, MA, LA, AZ, RI, AR, CO, WY, OH, IN, MO, NJ, MD, CT, WA, PA, UT, VA, NM, ME, MN, DC, TN, NE, OR, ND, WV.",
      "openfda": {
        "k_number": [
          "K100811",
          "K230530",
          "K143310",
          "K253224",
          "K220557",
          "K080825",
          "K180126",
          "K050415",
          "K130338",
          "K172122"
        ],
        "device_name": "Monitor, Extracellular Fluid, Lymphedema, Extremity",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.2770",
        "device_class": "2",
        "registration_number": [
          "3005699942",
          "3003695829",
          "3004896338",
          "3003857828",
          "3004782476"
        ],
        "fei_number": [
          "3005699942",
          "3003695829",
          "3004896338",
          "3003857828",
          "3004782476"
        ]
      }
    }
  ]
}