Company: Siemens Medical Solutions USA, Inc
Date of Enforcement Report: 1/8/2026
Class: II
PRODUCT:
LUMINOS Lotus Max, Model 11574100 and Luminos dRF Max, Model 10762471
Recall Number:
Z-0999-2026
REASON:
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.
RECALLING FIRM/MANUFACTURER:
Siemens Medical Solutions USA, Inc
VOLUME:
U.S.: 1, OUS: 95
DISTRIBUTION:
U.S. and OUS
