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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.
See this for other years:
2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2025
2026
  • 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.
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