WhichRecall
Class IIReported 2026-01-14

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

Recalled by Siemens Medical Solutions USA, Inc

Reason for Recall

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.

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Recall Number
Z-0999-2026
Classification
Class II
Status
Ongoing
Category
device
Initiated
2025-12-05
Reported
2026-01-14
Distribution
U.S. and OUS
Code Info
(01)04056869269931(21)10330
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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