{
  "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": "Terminated",
      "city": "Louisville",
      "state": "CO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89570",
      "recalling_firm": "Bolder Surgical, LLC",
      "address_1": "331 S 104th St",
      "address_2": "Suite 200",
      "postal_code": "80027-9713",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: NY, MO, DE, PA, FL     OUS: Italy, Chile, UK",
      "recall_number": "Z-0736-2022",
      "product_description": "CoolSeal Generator, REF: CSL-200-50",
      "product_quantity": "10",
      "reason_for_recall": "A potential manufacturing/assembly defect could result in the generator not meeting IEC 60601 standards for medical electrical equipment, and it can potentially, under specific conditions, lead to the delivery of unintended energy to the patient.",
      "recall_initiation_date": "20220125",
      "center_classification_date": "20220308",
      "termination_date": "20240515",
      "report_date": "20220316",
      "code_info": "Serial Numbers: 00161-170, UDI: 00850346007023"
    }
  ]
}