FDADecember 5, 2025device

LUMINOS Lotus Max, Model 11574100 and Luminos dRF Max, Model 10762471

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

The hazard

A potential issue associated with LUMINOS Lotus Max and Luminos dRF Max systems with software version VF11 with bucky wall stand for mobile detectors and without ceiling stand .When switching quickly between organ programs (OGPs) the collimation may be incorrect.

What to do

FDA enforcement status: Ongoing

Brands named

siemens medical solutionssiemenssiemens medical

UPCs

04056869269931

Recall history

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

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