FDAMarch 12, 2019device

Elekta Unity, Image-Guided Radiation Therapy System Product Usage: Elekta Unity using Magnetic Resonance Imaging is indicated for radiation therapy treatments and stereotactic radiation treatments of malignant and benign diseases anywhere in the body as determined by a licensed medical practition...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Users need to be aware when using these protocols for daily on line plan adaptation that: 1) The images acquired using these protocols do not represent the average position of the anatomy during the respiratory motion cycle. The images are based on data acquired around full expiration. 2) The display of the images in the Elekta Unity Application software does not provide information about the protocol used to acquire the image eg. with or without respiratory triggering. Users must select an appropriate scan protocol that is representative of the respiratory phase used in the reference plan.

What to do

FDA enforcement status: Terminated

Brands named

elekta

UPCs

30004070001

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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