HIGH
FDA DEVICE
Brand Name: Leksell Vantage Arc System REF: 1053958
Locking mechanisms may not properly secure to the Arc system, resulting in shifting of coordinates during procedures.
Elekta
Locking mechanisms
Elekta Recalls
5 recalls found for Elekta. Check if any of your products are affected.
Health & Personal Care
HIGH
FDA DEVICE
Elekta Recalls Medical Linear Accelerators Due to Grounding Issues
Elekta recalled 5,391 medical linear accelerators on December 14, 2025. A manufacturing issue related to electrical grounding poses a serious hazard. Patients and healthcare providers must stop using these devices immediately.
Elekta
Due to
Health & Personal Care
HIGH
FDA DEVICE
Elekta Recalls Radionuclide RT Treatment Planning System Over High-Risk Error
Elekta recalled the Leksell GammaPlan RT Treatment Planning System on December 12, 2025, due to a software error. This defect may lead to incorrect patient irradiation if not detected. Healthcare providers must stop using the software immediately.
Elekta
Due to
Health & Personal Care
HIGH
FDA DEVICE
Elekta Recalls Leksell GammaPlan Software Due to High Radiation Risks
Elekta recalled the Leksell GammaPlan Radionuclide RT Treatment Planning System on December 12, 2025. The software, used for treatment planning, may incorrectly irradiate patient locations due to a stereotactic reference error. This recall affects users worldwide, including in the U.S. and various international locations.
Elekta
Due to
Health & Personal Care
HIGH
FDA DEVICE
Elekta Recalls MOSAIQ Oncology System Over Overtreatment Risk
Elekta recalled the MOSAIQ Oncology Information System on December 10, 2025. A malfunction may cause overtreatment in patients due to software issues. Healthcare providers should stop using the device immediately and follow recall instructions.
Elekta
Using oncology
Brand Statistics
Total Recalls
5
Pages
1