Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Siemens Luminos dRF Fluoroscopic X-Ray system Fluoroscopic X-Ray system Recalled by Siemens Medical Solutions USA, Inc Due to Siemens became aware of an unintended behavior when...
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
Siemens Luminos dRF Fluoroscopic X-Ray system Fluoroscopic X-Ray system
Quantity: 4
Why Was This Recalled?
Siemens became aware of an unintended behavior when using the Luminos dRF with software version VD10A. The possibility exists that a software error may occur causing the table to tilt into an upright position and may collide with the floor. Four consignees were notified of this recall by Update Instruction XP067/12/S -- all four units have been corrected.
Where Was This Sold?
This product was distributed to 4 states: CA, IN, NJ, OK
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