Elekta ERGO++ Medical Device Recall for Incorrect DICOM Mapping
Elekta Inc is recalling 182 ERGO++ devices due to incorrect DICOM mapping of collimator or couch angles, which may lead to incorrect rotation during planning.
- Product
- Elekta ERGO++ Product Usage: ERGO is often used for stereotactic treatments.
- Category
- Medical Device
- Distribution
- Distributed nationwide