Reported Jan 29, 2014 · Terminated

SIMVIEW NT and SIMVIEW NT with IDI: October 01, 2012 Siemens ceased Simview distribution. Manufactured by: Mecaserto…

Siemens Medical Solutions USA, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Siemens Medical Solutions USA, Inc · 757 Arnold Dr Ste A · Martinez, CA · 94553-3615

Is this the product you have?

  • SIMVIEW NT and SIMVIEW NT with IDI
    • October 01
    • 2012 Siemens ceased Simview distribution
  • Manufactured byMecaserto 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
Lot codes and dates
  • SIMVIEW NT Part number5496992
  • SIMVIEW NT with IDI Part number5497016
  • US Serial numbers6019 6029 6032 6035 6068 6080 6001
  • International serial numbers
    • 6060
    • 6027
    • 6067
    • 1236
    • 3654
    • 4190
    • 6006
    • 6007
    • 6014
    • 6015
    • 6020
    • 6022
    • 6023
    • 6024
    • 6030
    • 6042
    • 6048
    • 6049
    • 6053
    • 6054
    • 6062
    • 6065
    • 6069
    • 6070
    • 6084
    • 6085
    • 6088
    • 6092
    • 6095
    • 6098
    • 6099
    • 6103
    • 6104
    • 6041DEL
    • 6099-1
    • 1256
    • 6017
    • 6028
    • 6034
    • 6036
    • 6041
    • 6044
    • 6047
    • 6050
    • 6052
    • 6055
    • 6056
    • 6058
    • 6066
    • 6072
    • 6073
    • 6079
    • 6082
    • 6083
    • 6089
    • 6090
    • 6093
    • 6105
Amount recalled
65 active devices

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

Why it was 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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Mar 31, 2014 · Data as of Sep 19, 5:21 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.