{
  "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": "2026-04-15",
    "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": "73364",
      "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 : TX, MD, MI, CA, TN, NH, NY, AL, NC, ID, MA, AZ, IN, FL, PA, NJ, WI, VA, MN, MD CO, GA, SC, OH and DC.",
      "recall_number": "Z-1231-2016",
      "product_description": "GE Inspection Technologies, LP, Cabinet X-ray system used for industrial quality control.",
      "product_quantity": "55 US Distribution",
      "reason_for_recall": "GE Inspection Technologies, LP (\"GE\") has discovered that certain of its cabinet x-ray systems may not fully comply with the Food and Drug Administration's (FDA) Cabinet X¿ ray System  performance  standards,  21  C.F.R.  ¿  1020.40(c)(1)(i)",
      "recall_initiation_date": "20151216",
      "center_classification_date": "20160401",
      "termination_date": "20161014",
      "report_date": "20160413",
      "code_info": "phoenix micrornelx and nanomelx cabinet x-ray systems",
      "more_code_info": ""
    }
  ]
}