{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Jinan",
      "state": "",
      "country": "China",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96035",
      "recalling_firm": "Jinan Bodor Cnc Machine Co Ltd",
      "address_1": "NO.1299, XINLUO AVE HI-TECH ZONE",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-0768-2025",
      "product_description": "Bodor P and C series laser cutting machines",
      "product_quantity": "269 units",
      "reason_for_recall": "Non-compliant laser products",
      "recall_initiation_date": "20241219",
      "center_classification_date": "20250118",
      "report_date": "20250129",
      "code_info": "P series is 2421537-000 and C series is 2421612-000.",
      "more_code_info": ""
    }
  ]
}