{
  "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": "2026-04-01",
    "results": {
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      "city": "Lake Oswego",
      "state": "OR",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87549",
      "recalling_firm": "BIOTRONIK Inc",
      "address_1": "6024 Jean Rd",
      "address_2": "N/A",
      "postal_code": "97035-5571",
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      "product_description": "BIOTRONIK INTICA NEO 7 HF-T DF-1 IS-1 ProMRI, REF 429553, UDI: 04035479156831 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.",
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      "reason_for_recall": "There is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds)",
      "recall_initiation_date": "20210308",
      "center_classification_date": "20210421",
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      "report_date": "20210428",
      "code_info": "Serial Number  84737505  84737521  84738497  84738498  84738995  84738997  84739001  84739004",
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