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Siemens Medical Solutions USA, Inc recalls Mevatron M2/Primus Mid-Energy PRIMUS HI
Recalled March 29, 2017 · FDA recall Z-1489-2017 · Siemens Medical Solutions USA
Hazard
Software update · FDA Class II
Units
80 systems
Sold at
Distributed throughout the United States
Description
Software update
Product
Mevatron M2/Primus Mid-Energy PRIMUS HI
Manufacturer(s)
Siemens Medical Solutions USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →