LUMINOS Lotus Max, Model 11574100 and Luminos dRF Max, Model 10762471
Reported: January 14, 2026 Initiated: December 5, 2025 #Z-0999-2026
Product Description
LUMINOS Lotus Max, Model 11574100 and Luminos dRF Max, Model 10762471
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.
Details
- Recalling Firm
- Siemens Medical Solutions USA, Inc
- Units Affected
- U.S.: 1, OUS: 95
- Distribution
- U.S. and OUS
- Location
- Malvern, PA
Frequently Asked Questions
What product was recalled? ▼
LUMINOS Lotus Max, Model 11574100 and Luminos dRF Max, Model 10762471. Recalled by Siemens Medical Solutions USA, Inc. Units affected: U.S.: 1, OUS: 95.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 14, 2026. Severity: Moderate. Recall number: Z-0999-2026.
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