FDAApril 30, 2020device

Elekta Unity, UDI 05060191071321, Image-guided radiation therapy system - Product Usage: 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 ...

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

The hazard

potential risk that Legionella may be present in the Unity machine room, specifically the heat exchanger condensation collection tray.

What to do

FDA enforcement status: Terminated

Brands named

elekta

UPCs

05060191071321

Recall history

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

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →