FDAFebruary 9, 2026device

RefleXion X1 Radiotherapy System Model RXM1000, Part #800-00006-00

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

The hazard

Due to a radiotherapy medical system software defect, when performing angular roll corrections followed by a repeat localization, the roll corrections applied in the initial localization scan are not carried through to treatment delivery leading to the treatment plan dose being delivered to the incorrect location, potentially a displacement of 5mm or higher, with a 10% to 20% underdose.

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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