Reported Sep 22, 2021 · Ongoing

syngo.CT VA20A, VA30A and VA40A in: syngo.via RT Image Suite / Sim&Go SOMATOM go.Now SOMATOM go.Up SOMATOM go.All…

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 · 40 Liberty Blvd · Malvern, PA · 19355-1418

Is this the product you have?

  • syngo.CT VA20A
  • VA30A and VA40A insyngo.via RT Image Suite / Sim&Go SOMATOM go.Now SOMATOM go.Up SOMATOM go.All SOMATOM go.Top SOMATOM go.Sim SOMATOM go.Open Pro and SOMATOM X
  • cite Material Numbers11061620 11061628 11061630 11061640 11061660 11061670
Lot codes and dates
  • Serial Numbers
    • 128051
    • 130051
    • 128065
    • 128035
    • 130057
    • 128086
    • 128079
    • 128041
    • 128019
    • 128078
    • 128060
    • 128068
    • 112045
    • 128085
    • 128075
    • 128022
    • 128033
    • 130012
    • 128016
    • 130044
    • 130048
    • 130049
    • 128018
    • 119216
    • 108085
    • 128015
    • 130019
    • 130055
    • 130054
    • 128020
    • 128039
    • 130052
    • 130036
    • 130061
    • 128049
    • 117756
    • 128029
    • 130021
    • 130045
    • 130039
    • 128063
    • 128057
    • 128045
    • 128046
    ***UPDATED 12/9/21*** 128114 128113 130058 ***Updated 1/31/22: Serial Number
    • 128123
    • 130015
    • 130081
    • 112261
    • 112071
    • 128124
    • 128132
    • 128125
    • 130079
    • 130077
  • Expanded Recall 3/12/2211061620
  • S/N111805 11061660
  • S/N
    • 128144
    • 128135
    • 128142
    • 128136
    • 128133 11061670
  • S/N
    • 130088
    • 130094
    • 130090
    • 130087
    • 130091
    • 130092
    • 130089
Amount recalled
44 systems

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

  • Nationwide

Why it was recalled

Potential for data loss when using the contouring or patient marking workflow when editing a structure set after saving and reopening a study, resulting in an incomplete structure set sent to the treatment planning system (TPS).

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

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:39 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.