{
  "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": "2026-08-13",
    "results": {
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    {
      "cfres_id": "29848",
      "product_res_number": "Z-0076-04",
      "event_date_initiated": "2003-09-24",
      "event_date_posted": "2003-10-31",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-02-17",
      "res_event_number": "27418",
      "product_code": "LWS",
      "pma_numbers": [
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      "code_info": "Serial Numbers:  7811xxxx",
      "firm_fei_number": "1028232",
      "recalling_firm": "Biotronik Inc",
      "address_1": "6024 Jean Road",
      "city": "Lake Oswego",
      "state": "OR",
      "postal_code": "97035-5369",
      "additional_info_contact": "800-547-0394 Ext. 394",
      "reason_for_recall": "Potential for early depletion of Implantable Cardioverter Defibrillator battery.",
      "root_cause_description": "Other",
      "action": "Firm issued a letter dated September 24, 2003 recommending physicians schedule an immediate follow-up to reprogram the affected devices.",
      "product_quantity": "794 devices",
      "distribution_pattern": "The firm distributes to physicians located throughout the US.",
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        "device_name": "Implantable Cardioverter Defibrillator (Non-Crt)",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
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}