Every recall we track for Elekta Limited — 6 in all — plus the complaints and injury reports the public filed about them.
Elekta recalls specific software versions for Unity system due to potential contour data mismatch in motion monitoring workflows, which could affect treatment accuracy.
Elekta recalls Unity MRI systems due to unvalidated use of gadolinium contrast agents in radiation therapy. Affected units may pose risks if contrast agents are administered without proper validation.
Elekta recalls Unity radiation therapy systems using MRI for potential image misalignment during respiratory motion. Users must select correct scan protocols to avoid treatment errors.
Elekta recalls Unity devices with specific serial numbers due to rare risk of speakers becoming dislodged and pulled into the bore during use, potentially causing injury.
Elekta recalls Agility with Integrity R3.2 devices due to potential positional errors when automatic table movement occurs. Affected units have product code 90I--YE and no serial numbers.
Elekta recalls Integrity R1.2 devices with potential positional errors after automatic table movement. Affected units have product code 90I--YE. No serial number.
