{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Sylmar",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89825",
      "recalling_firm": "St. Jude Medical, Cardiac Rhythm Management Division",
      "address_1": "15900 Valley View Ct",
      "address_2": "",
      "postal_code": "91342-3577",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the states of  FL, KY and the country of France, Czech Republic.",
      "recall_number": "Z-0989-2022",
      "product_description": "Gallant VR Implantable Cardioverter Defibrillator  REF # CDVRA500Q",
      "product_quantity": "2",
      "reason_for_recall": "Bluetooth malfunction impacting Gallant devices post-implant. The failure causes the device to  enter an inductive-only telemetry mode with a loss of Bluetooth communication. The Bluetooth malfunction results in the inability to remotely monitor these devices and resulted in reduced battery longevity.",
      "recall_initiation_date": "20220310",
      "center_classification_date": "20220421",
      "report_date": "20220427",
      "code_info": "REF# CDVRA500Q  SN: 111009251, Exp Date : 31-Jul-2022, Material # 100173801;   SN # 810000544, Exp Date: 31-Oct-2022, Material # 600115400  UDI# 05415067031990",
      "more_code_info": ""
    }
  ]
}