{
  "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": "2026-09-12",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "217655",
      "product_res_number": "Z-0888-2026",
      "event_date_initiated": "2025-09-30",
      "event_date_posted": "2025-12-31",
      "recall_status": "Open, Classified",
      "res_event_number": "98118",
      "product_code": "RFE",
      "product_description": "Material Processing Laser Products",
      "code_info": "N/A",
      "firm_fei_number": "3021692431",
      "recalling_firm": "SHENZHEN ATOMSTACK TECHNOLOGIES",
      "address_1": "3 Baolong 6 Rd",
      "state": "Guangdong",
      "country": "China",
      "reason_for_recall": "Lack of Remote Interlock Connector - required per 21 CFR 1040.10(f)(3)",
      "root_cause_description": "Radiation Control for Health and Safety Act",
      "action": "CAP letter to be sent to customers.",
      "distribution_pattern": "U.S.",
      "openfda": {
        "device_name": "Laser Cutter",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "N"
      }
    }
  ]
}