{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Hasselager",
      "state": "N/A",
      "country": "Denmark",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92230",
      "recalling_firm": "NRT X-RAY A/S",
      "address_1": "Birkegardsvej 16",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of OH, NC, KY, SC, IA, MA, WA, LA, NV, NY.",
      "recall_number": "Z-1668-2023",
      "product_description": "Intelli-C, Right side suspended Tabletop, REF: 03400000",
      "product_quantity": "32 units",
      "reason_for_recall": "There is a potential that the drive shaft in the detector up/down (IDE) movement of the X-Ray machine may break which causes  the detector  to move until it is stopped by the movement end-stop.",
      "recall_initiation_date": "20230427",
      "center_classification_date": "20230531",
      "report_date": "20230607",
      "code_info": "UDI-DI: 05713464000527/Serial Numbers: 627004, 627007, 639001, 639002,639003, 639004, 639007, 639010, 647001, 647004, 647005, 648001, 651007, 658002, 658003, 658006, 658010, 666008, 675001, 675004, 682006, 682010"
    }
  ]
}