Philips Ingenia Blue Seal MRI Systems Recalled for DTI Export Errors
Philips is recalling six Ingenia Blue Seal MRI systems because diffusion tensor imaging exports contain incorrect data, preventing accurate tractography reconstruction.
- Product
- Ingenia Blue Seal SE and Blue Seal XE; Model number (REF): 1. 782185 (SE), 2. 782192 (XE); Software Versions: R11, R12 and R13;
- Category
- Medical Device
- Distribution
- Distributed nationwide