{
  "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": [
    {
      "country": "United States",
      "city": "Waukesha",
      "address_1": "3000 N Grandview Blvd",
      "reason_for_recall": "GE Healthcare has become aware of a software issue on the interface of the mobile radiographic product, Optima XR200amx, ond Optima XR220amx related to Visual indication as mandated by the US Code of Federal Regulations (21CFR) and IEC 60601-1-3.",
      "address_2": "",
      "product_quantity": "254 units have been shipped to/installed in the U.S.",
      "code_info": "Model Numbers  Optima XR200 15kw  Optima XR 200 30kw  Optima XR 220 15kw  Optima XR 220 30kw",
      "center_classification_date": "20120719",
      "distribution_pattern": "Worldwide Distribution (USA) nationwide",
      "state": "WI",
      "product_description": "GE Healthcare Optima Mobile X-ray System.  The GE Automatic Mobile X-Ray   (AMX ) Series are intended to take exposures utilizing film or computed radiography ( CR )",
      "report_date": "20120725",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "GE Healthcare, LLC",
      "recall_number": "Z-1993-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "62527",
      "termination_date": "20130110",
      "more_code_info": "",
      "recall_initiation_date": "20120404",
      "postal_code": "53188-1615",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}