FDA recall Z-1656-2026

Reflexion Medical, Inc. · Class II · device

Product

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

Reason for recall

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.

Distribution

US: CA, TX, PA, CT, NJ, OR, LA, OH

Key facts

Status
Ongoing
Initiation date
2026-02-09
Report date
2026-04-08
Voluntary/Mandated
Voluntary: Firm initiated
Location
Hayward, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1656-2026