{
  "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": "Lewistown",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69849",
      "recalling_firm": "GE Inspection Technologies, LP",
      "address_1": "50 Industrial Park Rd",
      "address_2": "N/A",
      "postal_code": "17044-9312",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the states of : NY, CA, WA, PA, MD, AL, FL and LA.",
      "recall_number": "Z-2320-2015",
      "product_description": "GE Optional Laser Centering Device  X-ray generator.",
      "product_quantity": "25",
      "reason_for_recall": "GE has identified a potential failure to comply with 21 C.F.R. ¿ 1040.10 and 21 C.F.R. ¿ 1010.2 for the alignment laser centering device.",
      "recall_initiation_date": "20141110",
      "center_classification_date": "20150813",
      "termination_date": "20170201",
      "report_date": "20150819",
      "code_info": "Model No. 025.03.00A"
    }
  ]
}