Deerfield Imaging Intra operative MRI Systems: Neuro II-SE , Neuro III-SV, iMRI 1.5T A, and recall — FDA Z-1098-2016
Emergency helium venting lines (i.e. quench lines) may not have been properly installed.
Overview of recall records associated with Deerfield Imaging, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Emergency helium venting lines (i.e. quench lines) may not have been properly installed.
This page summarizes recall records in which the official source identifies Deerfield Imaging as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.