FDAApril 3, 2019device

Elekta Unity systems 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 practitioner in accordance with a defined...

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

The hazard

There is no warning in the Elekta Unity manual for the administration of gadolinium-based or other contrast agents for imaging or image guidance purposes has not been validated.

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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