{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Salt Lake City",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71298",
      "recalling_firm": "GE OEC Medical Systems, Inc",
      "address_1": "384 N Wright Brothers Dr",
      "address_2": "N/A",
      "postal_code": "84116-2862",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the states of: MD, NC, MT, NJ, UT and NY",
      "recall_number": "Z-1638-2015",
      "product_description": "GE OEC Brivo 865 plus, Mobile X-ray system laser aimer assemblies (part number 520002DW)",
      "product_quantity": "9",
      "reason_for_recall": "Laser aimer assemblies were shipped without certification of the overall assembly or submitting a laser product report and therefore do not comply with the US regulations for laser products.",
      "recall_initiation_date": "20140522",
      "center_classification_date": "20150608",
      "termination_date": "20150624",
      "report_date": "20150617",
      "code_info": "OEC Brivo 865 Plus serial numbers B4S13061, B4S14006, B4S14007, B4S13033, B4S13032, B4S13038, B4S13039, B4S13024, AND B4S13023."
    }
  ]
}