[Recalled] LUMINOS Lotus Max, Model 11574100 and Luminos dRF Max, Model 10762471 — A potential issue associated with LUMINOS Lotus Max and Luminos dRF Max systems… | FDA 2025-12-05
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | LUMINOS Lotus Max, Model 11574100 and Luminos dRF Max, Model 10762471 |
|---|---|
| Brand / manufacturer | Siemens Medical Solutions USA, Inc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0999-2026 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 05 December 2025 |
| EAN / barcode | 04056869269931 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: 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.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Siemens Medical Solutions USA, Inc
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.