{
  "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,
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "Shelton",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83295",
      "recalling_firm": "Comet Technologies Usa Inc",
      "address_1": "100 Trap Falls Rd",
      "address_2": "N/A",
      "postal_code": "06484-4604",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-2105-2019",
      "product_description": "YXLON Cheetah cabinet X-Ray System    Product Usage:  The products are generally used for non-destructive testing and quality control",
      "product_quantity": "77",
      "reason_for_recall": "Failure to meet the requirement of the performance standard for cabinet x-ray systems (21 CFR 1020.40) for a door interlock that causes physical disconnection of the power supply using only the movement of the door.",
      "recall_initiation_date": "20181001",
      "center_classification_date": "20190807",
      "termination_date": "20240613",
      "report_date": "20190814",
      "code_info": "X-Ray Systems"
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}