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Recall Observatory FDA recall evidence

Device product

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

Z-1164-2013

October 06, 2011

Class II

Product summary

Firm
GE Healthcare, LLC
Event
Event 64804
Status
Terminated
Classification
Class II
Quantity
11
Official record key
device-enforcement:Z-1164-2013

Official wording

Reason: 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.

Code information: Mfg Lot or Serial # 0000CZC7105FJM000 00000CZC827NRN000 00000CZC8283V4000 0000CZC8283V47000 0000CZC8283V72001 0000CZC8283TX5001 00000000211423001 0000CZC8161XJT000 0000CZC94154WV003 0000CZC83942HL000 0000CZC8396CC9001

Distribution pattern: Worldwide Distribution - USA including GA, and NY; and countries of: Canada, Israel, Italy and Switzerland.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software issue

Field note

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