{
  "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": "2026-04-22",
    "results": {
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      "limit": 1,
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  "results": [
    {
      "country": "United States",
      "city": "Sylmar",
      "address_1": "15900 Valley View Ct",
      "reason_for_recall": "New pacemaker firmware was developed to further mitigate the risk of unauthorized access to our pacemakers that utilize radio frequency (RF) communications.",
      "address_2": "",
      "product_quantity": "101 units",
      "code_info": "Serial Numbers: 2736872  2736871  2736870  2736874  2736873  2538305  2538304  2538301  2538306  2538307  2538302  2512808  2512812  2512811  2384089  2512807  2384108  2384112  2397881  2393253  2393254  2401631  2512803  2401623  2401617  2512810  2384086  2384126  2384101  2384122  2384121  2384105  2384096  2384098  2384116  2384110  2384111  2384120  2384082  2384085  2384123  2384124  2384107  2384117  2384087  2384097  2384077  2393264  2384115  2384119  2384114  2384104  2384100  2384078  2384092  2384081  2384084  2397878  2401620  2384080  2384079  2384099  2401621  2401624  2384083  2512819  2512818  2401626  2401622  2397879  2397872  2393252  2393259  2401619  2401618  2401629  2397874  2397880  2401628  2384106  2393255  2393256  2393257  2512802  2512805  2512800  2512817  2512801  2512804  2512813  2512814  2512815  2512816  2512806  2512809  2384102  2384095  2384125  2384113  2384103  2393262",
      "center_classification_date": "20171019",
      "distribution_pattern": "Worldwide Distribution",
      "state": "CA",
      "product_description": "PM1226 ACCENT ST MRI SR RF and PM2222 ACCENT ST  These low voltage (LV) devices are implantable pacemaker pulse generators, intended to be permanently implanted in the body, that have a power supply and electronic circuits that produce a periodic electrical pulse to stimulate the heart.  These devices are used as a substitute for the heart's intrinsic pacing system to correct both intermittent and continuous cardiac rhythm disorders.",
      "report_date": "20171025",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "St Jude Medical Inc.",
      "recall_number": "Z-0035-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "78093",
      "termination_date": "20200708",
      "more_code_info": "",
      "recall_initiation_date": "20170828",
      "postal_code": "91342-3577",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}