{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Skaneateles Falls",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86620",
      "recalling_firm": "Ge Inspection Technologies Llc",
      "address_1": "721 Visions Dr",
      "address_2": "N/A",
      "postal_code": "13153-5314",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "USA  Canada",
      "recall_number": "Z-0442-2021",
      "product_description": "v|tome|x L Series non-destructive testing cabinet x-ray systems",
      "product_quantity": "N/A",
      "reason_for_recall": "It was discovered during testing of  the v/tome/x L450 system s/n PA1790, that the pre-warning signals does not provide \"Audible and visible warning signals within the cabinet\" if the \"warm up\" mode was not completed after initializing the system when first turned on.",
      "recall_initiation_date": "20200929",
      "center_classification_date": "20201113",
      "termination_date": "20230502",
      "report_date": "20201125",
      "code_info": "v/tome/x  L Series (L240, L300 or L450)"
    }
  ]
}