Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SIMVIEW NT and SIMVIEW NT with IDI: October 01 Recalled by Siemens Medical Solutions USA, Inc Due to In a very rare occurrence an intended movement...
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
SIMVIEW NT and SIMVIEW NT with IDI: October 01, 2012 Siemens ceased Simview distribution. Manufactured by: Mecaserto now known as Mecasim Parc de lEsplanade 9,Rue Niels Bohr 77400 Saint Thibault des Vignes- France The intended use of the SIEMENS branded SIMVIEW NT and SIMVIEW NT with IDI is a radiation therapy simulation system.
Quantity: 65 active devices
Why Was This Recalled?
In a very rare occurrence an intended movement of the SimView NT simulation system components could not be stopped with usual hand control or the collision detection functionality.
Where Was This Sold?
Class II Recall - Worldwide Distribution - US Distribution including the states of California, Louisiana, Massachusetts, Pennsylvania, New York, Kentucky and Michigan., and the countries of Bulgaria, Germany, Belarus, Russian Fed., P.R. China, India, Republic Korea, Germany, Costa Rica, Argentina, Portugal, Greece, Bulgaria, Vietnam, Hungary, Italy, Palestinian Ter, Hungary, Jordan, Egypt Poland, Greece, Curacao, St Eus, Malaysia, Egypt, Malaysia, South Africa Turkey, Thailand, Qatar and Iraq.
About Siemens Medical Solutions USA, Inc
Siemens Medical Solutions USA, Inc has 20 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report