{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Sylmar",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80212",
      "recalling_firm": "St Jude Medical Inc.",
      "address_1": "15900 Valley View Ct",
      "address_2": "",
      "postal_code": "91342-3577",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S. Nationwide distribution",
      "recall_number": "Z-2329-2018",
      "product_description": "Merlin PCS programmer (Model # 3650), Software (Model # 3330)",
      "product_quantity": "71651",
      "reason_for_recall": "The firm is releasing new firmware for high voltage implantable cardiac devices (ICD) and cardiac resynchronization therapy defibrillators (CRT-D) intended to strengthen security by providing an additional layer of protection against unauthorized device access. For older generation devices not capable of accepting the firmware, the firm is advising customers of the option to permanently disable the RF communication capability in these devices.",
      "recall_initiation_date": "20180416",
      "center_classification_date": "20180628",
      "termination_date": "20240308",
      "report_date": "20180704",
      "code_info": "Software Versions: 24.1.1 rev1 (US), 23.1.2 rev 1 (OUS), 23.1.3 (Japan), and 23.1.4 rev 1 (Canada)",
      "more_code_info": ""
    }
  ]
}