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Recall Observatory FDA recall evidence

Device product

Siemens Luminos dRF, Ysio or Uroskop Omnia systems. The Axiom Luminos dRF is intended to be used as a universal diagnostic imaging system for radiographic and fluoroscopic studies.

Z-2292-2014

July 07, 2014

Class II

Product summary

Firm
Siemens Medical Solutions USA, Inc
Event
Event 68785
Status
Terminated
Classification
Class II
Quantity
192
Official record key
device-enforcement:Z-2292-2014

Official wording

Reason: It was discovered that during a RAD examination using Siemens Luminos dRF, Ysio or Uroskop Omnia systems with software version VB10C to VB10F and automatic exposure control, a highly unlikely malfunction can result in longer radiation exposure than required. This may also result in an overexposed image that is not of diagnostic quality. As a result the taken examination needs to be repeated. Thi

Code information: model numbers 10094200, 10281163, 10281013, 10094910 with multiple serial numbers

Distribution pattern: Nationwide Distribution.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software version VB10C to VB10F and automatic exposure control, a highly unlikely malfunction can result in