Elekta, Inc.: Medical Device Recalls in 2013
Updated on March 25, 2026.
According to to data from the FDA, there were 9 medical device recalls made by Elekta, Inc. in 2013. See the details of the recalls below.
You can see similar recalls for other firms.
Data Source: FDA.
- Integrity 3.0 Product Usage: The Agility multileaf collimator is indicated for use when additional flexibility is required in conforming the radiation beam to the anatomy to be exposed.
- DMLC IV-ERGO - Beam shaping block for Radiation Therapy.
- Precise Treatment Table. To be used as part of radiation therapy treatment process.
- Elekta Synergy XVI. Radiation Therapy Digital Imager. Product XVI R3.5.1, R4.2.1, and R4.5.1 Used as part of radiation therapy treatment process.
- Elekta, Apex add-on Micro MLC, collimator for radiation therapy.
- Monaco RTP System. Radiation treatment planning.
- Monaco RTP System Radiation Therapy Treatment Planning System. Radiation treatment planning.
- Monaco RTP System Radiation treatment planning
- Stereotactic Circular Collimator - 3D Line stereotatic Hardware Accessories The device is part of the class of medical devices that are used in radiotherapy for the treatments of head tumors.