FDAApril 16, 2024device

RefleXion X1 Radiotherapy System Model RXM1000 Software version 2.1.19-3 Radiation therapy system is a device that combines the functionality of an emission computed tomography detection system and a linear accelerator.

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

The hazard

A potential dose error exists for patients treated with an out of session SCINTIX partial fraction.

What to do

FDA enforcement status: Ongoing

Brands named

reflexion medicalreflexion

UPCs

00860003983812

Recall history

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

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