FDANovember 24, 2021device

RefleXion Medical Radiotherapy System - System Label: "*** refleXion REF RXM1000 ***" Physics Guide/Treatment Delivery User Manual/Treatment Planning User Manual: "RefleXion X1 Model: RXM1000"

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

The hazard

Due to dose discrepancy when delivering a plan to a patient in a Non-HFS (Head First Supine) orientation specifically in Feet First Supine (FFS).

What to do

FDA enforcement status: Terminated

Brands named

reflexion medicalreflexion

UPCs

00860003983805

Recall history

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

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