Home / Recalls / Medical Devices
Siemens Medical Solutions USA, Inc recalls MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643
Recalled August 28, 2019 · FDA recall Z-2344-2019 · Siemens Medical Solutions USA
Hazard
Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly. · FDA Class II
Units
2
Sold at
AL AR AZ CA CO CT DC DE FL GA GU IA ID IL IN KS KY LA MA MD ME MI MN MO MT NC NE NH NJ NY OH OK OR PA SC TN TX VA WA WI WV WY
Description
Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.
Product
MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643
Manufacturer(s)
Siemens Medical Solutions USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →