{
  "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": "2026-09-03",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 3
    }
  },
  "results": [
    {
      "cfres_id": "221738",
      "product_res_number": "Z-3081-2026",
      "event_date_initiated": "2026-08-06",
      "event_date_posted": "2026-09-02",
      "recall_status": "Open, Classified",
      "res_event_number": "99524",
      "product_code": "MXD",
      "k_numbers": [
        "K231328"
      ],
      "product_description": "LUX-Dx, LUX-Dx II, LUX-Dx II+ Insertable Cardiac Monitor System, SERVER SW LAT CLARITY DS US, Model Number 7260, All Versions (Current 7.8)",
      "code_info": "UDI-DI: 00802526613838",
      "firm_fei_number": "2124215",
      "recalling_firm": "Boston Scientific Corporation",
      "address_1": "4100 Hamline Ave N",
      "city": "Saint Paul",
      "state": "MN",
      "postal_code": "55112-5700",
      "reason_for_recall": "There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed notification of an AF Burden Alert may delay clinical evaluation or therapeutic intervention of an atrial arrhythmia.",
      "root_cause_description": "Software design",
      "action": "An Urgent Medical Device Correction dated August 2026 was sent to customers.\n\nBoston Scientific is notifying you of the potential for a delay in AF Burden Alert notification affecting the LATITUDE\" Clarity server software which supports the LUX-Dx\" family of ICMs. This delayed AF Burden Alert notification behavior by LATITUDE Clarity may occur if the Alert for AF Burden e Threshold is configured to \">0 hours per day\" setting (a non-default configuration).\nThe ICM is performing as intended with continued AF detection, data storage, and transmission of device data. Boston Scientific has received one complaint related to this delayed notification behavior by the LATITUDE Clarity System. No patient injuries or deaths have been reported. A server software update is planned to correct this behavior.\n\nConfiguration Options for Atrial Alert Notifications: Atrial arrhythmia alert notification preferences may vary, and AF configurations may be set for individual patients and/or group settings. Until updated server software is available, consider the following options:\nChange Threshold for AF Burden Alert Setting\nEnable AF Events Alert with Minimum Duration\nIf Unchanged, Potential Delay in AF Burden Alert Notification\n\" Boston Scientific does not recommend replacement of the implanted ICM.\n\" Please share this notification with all HCPs within your organization who manage patients using the LUXDx ICM and LATITUDE Clarity System.\n\nMitigation. The LATITUDE Clarity system is designed to detect atrial fibrillation through two independent mechanisms: AF Burden and AF Event Alerts. Until a software update to the LATITUDE Clarity server software is available, configuring AF Events or changing AF Burden Alerts settings can mitigate delays in full device interrogation and enable the LATITUDE Clarity system to display alert notification as intended.\n\nAdditional Information. The Regulatory Authority of your country has been informed of this communication. Adverse events should be reported",
      "distribution_pattern": "Worldwide - US Nationwide distribution.",
      "openfda": {
        "k_number": [
          "K132960",
          "K252593",
          "K193473",
          "K200795",
          "K201865",
          "K233320",
          "K211304",
          "K162855",
          "K210484",
          "K212008",
          "K261074",
          "K190548",
          "K171514",
          "K160809",
          "K253516",
          "K240693",
          "K223630",
          "K160689",
          "K233562",
          "K230553",
          "K231328",
          "K251221",
          "K150614",
          "K262735",
          "K132649",
          "K221856",
          "K163460",
          "K221962",
          "K230375",
          "K200444",
          "K143503",
          "K210608",
          "K170628",
          "K152995"
        ],
        "registration_number": [
          "9616693",
          "3008973940",
          "3009380063",
          "1028232",
          "9614453",
          "2124215",
          "2017865",
          "3015544746",
          "3004185781",
          "2182208",
          "9610139",
          "3018094310"
        ],
        "fei_number": [
          "3002806500",
          "3002618605",
          "3008973940",
          "3009380063",
          "1028232",
          "3002807576",
          "2124215",
          "2017865",
          "3015544746",
          "3004185781",
          "2182208",
          "3018094310"
        ],
        "device_name": "Recorder, Event, Implantable Cardiac, (With Arrhythmia Detection)",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.1025",
        "device_class": "2"
      }
    }
  ]
}