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Siemens Medical Solutions USA, Inc recalls Siemens syngo.plaza image processing system image processing radiological system
Recalled November 20, 2013 · FDA recall Z-0271-2014 · Siemens Medical Solutions USA
Hazard
The firm became aware of an unintended behavior when using the syngo.plaza. The "Rename" functionality can cause an unintended patient merge if the patient is sent to another system. This issue affects customers who transfer patient data between two or more syngo.plaza or syngo Imaging XS systems. · FDA Class II
Units
19
Sold at
Nationwide Distribution including MO, MA, NY, WI, OH, NY, CA, FL, NC, MN, and WA.
Description
The firm became aware of an unintended behavior when using the syngo.plaza. The "Rename" functionality can cause an unintended patient merge if the patient is sent to another system. This issue affects customers who transfer patient data between two or more syngo.plaza or syngo Imaging XS systems.
Product
Siemens syngo.plaza image processing system image processing radiological system
Manufacturer(s)
Siemens Medical Solutions USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →