Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Luminos dRF with software VD10- A diagnostic imaging system for Recalled by Siemens Medical Solutions USA, Inc Due to Potential risk of collision with the ceiling, wall,...
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 dRF with software VD10- A diagnostic imaging system for radiographic and fluoroscopic studies Model Number: 10094200
Quantity: 1 unit; Expanded Recall: 25 units
Why Was This Recalled?
Potential risk of collision with the ceiling, wall, or objects which may result in serious injury to staff or patients due to room configuration parameters of the system being set to default values
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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