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Siemens Medical Solutions USA, Inc recalls Siemens Luminos dRF Fluoroscopic X-Ray system Fluoroscopic X-Ray system
Recalled August 7, 2013 · FDA recall Z-1848-2013 · Siemens Medical Solutions USA
Hazard
Siemens became aware of an unintended behavior when using the Luminos dRF with software version VD10A. The possibility exists that a software error may occur causing the table to tilt into an upright position and may collide with the floor. Four consignees were notified of this recall by Update Instruction XP067/12/S -- all four units have been corrected. · FDA Class II
Units
4
Sold at
US Distribution including the states of CA, IN, NJ and OK.
Description
Siemens became aware of an unintended behavior when using the Luminos dRF with software version VD10A. The possibility exists that a software error may occur causing the table to tilt into an upright position and may collide with the floor. Four consignees were notified of this recall by Update Instruction XP067/12/S -- all four units have been corrected.
Product
Siemens Luminos dRF Fluoroscopic X-Ray system Fluoroscopic X-Ray system
Manufacturer(s)
Siemens Medical Solutions USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →