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Recall Observatory FDA recall evidence

Device product

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 defined treatment plan.

Z-2289-2020

April 30, 2020

Class II

Product summary

Firm
Elekta, Inc.
Event
Event 85651
Status
Terminated
Classification
Class II
Quantity
32 units
Official record key
device-enforcement:Z-2289-2020

Official wording

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

Code information: Serial numbers 600001 - 600043

Distribution pattern: Worldwide distribution - US Nationwide distribution including in the states of PA, WI, NY, TN, NJ, IA, TX, and the countries of Australia, Canada, China, Denmark, Germany, Hong Kong, Italy, Netherlands, Sweden, Switzerland, Thailand, Turkey, UK.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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