Drug recall
LUMINOS Lotus Max, Model 11574100 and Luminos dRF Max, Model 10762471
FDA recall event 98230 · Class II · Siemens Medical Solutions USA, Inc
Key facts
| Event ID | 98230 |
|---|---|
| Recall numbers | Z-0999-2026 |
| Recalling firm | Siemens Medical Solutions USA, Inc |
| Product type | Devices |
| Products | LUMINOS Lotus Max, Model 11574100 and Luminos dRF Max, Model 10762471 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | FDA Requested |
| 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… |
| Initiation date | Dec 5, 2025 |
| Report date | Jan 14, 2026 |
| City | Malvern |
| State | PA |
| Country | United States |
| FEI number | 2240869 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: