{
  "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": "2026-04-29",
    "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 in your Xeleris 2.1 workstation (that is used for processing Discovery 530/570 data), that may impact patient safety.    On imported CT scans, Myocardial Perfusion Imaging (MPI) studies may create artifacts in attenuation corrected images. This may lead to a potential for misdiagnosis.",
      "address_2": "",
      "product_quantity": "11",
      "code_info": "Mfg Lot or Serial #  0000CZC7105FJM000  00000CZC827NRN000  00000CZC8283V4000  0000CZC8283V47000  0000CZC8283V72001  0000CZC8283TX5001  00000000211423001  0000CZC8161XJT000  0000CZC94154WV003  0000CZC83942HL000  0000CZC8396CC9001",
      "center_classification_date": "20130423",
      "distribution_pattern": "Worldwide Distribution - USA including GA, and NY; and countries of: Canada, Israel, Italy and Switzerland.",
      "state": "WI",
      "product_description": "GE Healthcare, Xeleris 2 Processing & Review Workstation.    The display, processing, archiving, and communication of data acquired by Emission Tomography cameras used in diagnostic radiology, including procedures for planar imaging, whole body imaging, tomographic (SPECT) imaging, positron imaging by coincidence, attenuation correction, and anatomical image registration",
      "report_date": "20130501",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "GE Healthcare, LLC",
      "recall_number": "Z-1164-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64804",
      "termination_date": "20140204",
      "more_code_info": "",
      "recall_initiation_date": "20111006",
      "postal_code": "53188-1615",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}