{
  "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,
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  "results": [
    {
      "status": "Ongoing",
      "city": "Mounds View",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90429",
      "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": "Telephone",
      "distribution_pattern": "US Nationwide distribution in the states of Indiana and CA.",
      "recall_number": "Z-1480-2022",
      "product_description": "Cobalt Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT-D)",
      "product_quantity": "3 units",
      "reason_for_recall": "Manufacturing error that may have resulted in a cathode component being out of specification.  All devices met final functional testing requirements.",
      "recall_initiation_date": "20201105",
      "center_classification_date": "20220728",
      "report_date": "20220803",
      "code_info": "GTIN 00763000178178, Serial Numbers:  RTK601865S, RTK601825S, RTK601828S",
      "more_code_info": ""
    }
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}