Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LUMINOS Lotus Max Recalled by Siemens Medical Solutions USA, Inc Due to A potential issue associated with LUMINOS Lotus Max...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Siemens Medical Solutions USA, Inc directly.
Affected Products
LUMINOS Lotus Max, Model 11574100 and Luminos dRF Max, Model 10762471
Quantity: U.S.: 1, OUS: 95
Why Was This Recalled?
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.
Where Was This Sold?
U.S. and OUS
About Siemens Medical Solutions USA, Inc
Siemens Medical Solutions USA, Inc has 613 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report