Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MODULARIS VARIOSTAR Recalled by Siemens Medical Solutions USA, Inc Due to Display freeze of MODULARIS hand control results in...
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
MODULARIS VARIOSTAR; Lithotripter device designed to treat urolithiasis.
Quantity: 15
Why Was This Recalled?
Display freeze of MODULARIS hand control results in information not being updated on the display. Current treatment data is not shown to the user.
Where Was This Sold?
This product was distributed to 6 states: GA, KY, LA, MS, MO, NC
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