{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Lake Oswego",
      "state": "OR",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71658",
      "recalling_firm": "BIOTRONIK, Inc.",
      "address_1": "6024 Jean Rd",
      "address_2": "N/A",
      "postal_code": "97035-5571",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution.",
      "recall_number": "Z-2376-2015",
      "product_description": "PSW 1203.U/1, PSW 1301.U, PSW 1307.U, PSW 1403.U, and PSW 1501.U Pacemaker Programmer software.  Software approved for use with BIOTRONIK device programmers (trade names: Renamic and ICS 3000).    Allows physicians to program devices to pace exclusively in the left ventricle.",
      "product_quantity": "768  units (software)",
      "reason_for_recall": "Ventricular packing: LV software programming versions for  BIOTRONIK CRT-P and CRT-D devices are recalled because they are not approved for use in the US.",
      "recall_initiation_date": "20150630",
      "center_classification_date": "20150813",
      "termination_date": "20151224",
      "report_date": "20150819",
      "code_info": "Affected Product Part Numbers: 394229, 400335, 403222, 406797, 408849"
    }
  ]
}