{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Mounds View",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93663",
      "recalling_firm": "Medtronic Inc.",
      "address_1": "8200 Coral Sea St Ne",
      "address_2": "N/A",
      "postal_code": "55112-4391",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Visit",
      "distribution_pattern": "US Nationwide distribution in the state of Florida.",
      "recall_number": "Z-0779-2024",
      "product_description": "Cobalt XT DR MRI SureScan Implantable Cardioverter Defibrillator, product number DDPA2D1",
      "product_quantity": "1 device",
      "reason_for_recall": "During internal review of Polaris battery assembly data from the HiPot operation, a test systems engineer noticed that some batteries had gone through the High Potential test twice. This was able to occur because the test screen did not prevent retesting after a failure. Some batteries were therefore retested and passed.",
      "recall_initiation_date": "20231207",
      "center_classification_date": "20240122",
      "report_date": "20240131",
      "code_info": "UDI/DI 00763000178338, Serial Number RSL604096S"
    }
  ]
}