{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Mounds View",
      "state": "MN",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92328",
      "recalling_firm": "Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)",
      "address_1": "8200 Coral Sea St Ne",
      "address_2": "",
      "postal_code": "55112-4391",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide - Worldwide Distribution",
      "recall_number": "Z-1724-2023",
      "product_description": "ICD DDPA2D4G COBALT XT DR MRI DF4 GOLD, Model Number DDPA2D4G;  Implantable Cardioverter Defibrillators",
      "product_quantity": "6 units",
      "reason_for_recall": "There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glassed) feedthrough, including currently available ICDs and CRT-Ds.",
      "recall_initiation_date": "20230510",
      "center_classification_date": "20230616",
      "report_date": "20230628",
      "code_info": "GTIN 00763000615628, Lot Serial Numbers:  RSM616778S, RSM610606S, RSM611337S, RSM610608S, RSM611339S;  GTIN 00763000645502, Lot Serial Numbers:  RSM616777S",
      "more_code_info": ""
    }
  ]
}