Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PRIMUS Recalled by Siemens Medical Solutions USA, Inc Due to Software patch installation to address several safety issues.
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
PRIMUS, Accelerator, Linear, Medical The PRIMUSTM family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
Quantity: 103 accelerators
Why Was This Recalled?
Software patch installation to address several safety issues.
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