Class II
Medical Device Recall: Luminos dRF Max- Intended to visualize anatomical structures by converting an x-ray pattern into a visible image. Model Number: 10762471
Siemens Medical Solutions USA, Inc · July 2, 2024
Reason for Recall
The support arm may unintentionally lower resulting in injury to persons when they are under the display ceiling/wall suspension when positioning the displays
Distribution
US Nationwide distribution.
States Affected
NATIONWIDE
Quantity Affected
24 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2526-2024
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.