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Siemens Medical Solutions USA, Inc recalls Siemens Mobilett Mira mobile x-ray system Product Usage: Mobile x-ray system
Recalled September 19, 2012 · FDA recall Z-2367-2012 · Siemens Medical Solutions USA
Hazard
During regular product monitoring, firm became aware of a potential issue with the Mobilett Mira system, (serial numbers 1034, 1038, 1041, 1042, 1043, 1050, 1053, and 1054. During normal clinical operation the center screw on the driving wheel may become loose resulting in system immobilization. There is no risk of the system tipping over or collapsing on the floor, however the system may tilt t · FDA Class II
Units
9
Sold at
US Nationwide Distribution including the states of: GA, IA, KS, NC and TX.
Description
During regular product monitoring, firm became aware of a potential issue with the Mobilett Mira system, (serial numbers 1034, 1038, 1041, 1042, 1043, 1050, 1053, and 1054. During normal clinical operation the center screw on the driving wheel may become loose resulting in system immobilization. There is no risk of the system tipping over or collapsing on the floor, however the system may tilt t
Product
Siemens Mobilett Mira mobile x-ray system Product Usage: Mobile x-ray system
Manufacturer(s)
Siemens Medical Solutions USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →