FDA Flags Recall Involving IMRIS MRI Systems Linked to Siemens 3T Magnet Issue
The recall affects IMPRIS Neuro III-SV models that use Siemens 3T magnets, citing a risk of blocked helium venting during a magnet quench.
The recall affects IMPRIS Neuro III-SV models that use Siemens 3T magnets, citing a risk of blocked helium venting during a magnet quench.
Siemens Healthineers announces that it has obtained U.S. FDA clearance for the Somatom Pro.Pulse, a dual-source CT scanner intended for use in various healthcare facilities, including outpatient diagnostic centers.
The recall affects IMPRIS Neuro III-SV models that use Siemens 3T magnets, citing a risk of blocked helium venting during a magnet quench.