Reported Dec 1, 2021 · Terminated

SOMATOM Drive with software syngo.CT VB20 Model #10431700

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?

  • SOMATOM Drive with software syngo.CT VB20 Model #10431700
Lot codes and dates
  • Serial Numbers

    75 of 75 codes

    • 105081
    • 105478
    • 105152
    • 105471
    • 105315
    • 105484
    • 105182
    • 105228
    • 105207
    • 105128
    • 105123
    • 105241
    • 105105
    • 105020
    • 105063
    • 105035
    • 105022
    • 105045
    • 105052
    • 105150
    • 105485
    • 105302
    • 105472
    • 105096
    • 105477
    • 105047
    • 105023
    • 105180
    • 105115
    • 105086
    • 105295
    • 105398
    • 105051
    • 105196
    • 105445
    • 105336
    • 105383
    • 105402
    • 105202
    • 105046
    • 105109
    • 105244
    • 105498
    • 105466
    • 105461
    • 105165
    • 105060
    • 105464
    • 105103
    • 105121
    • 105141
    • 105344
    • 105066
    • 105503
    • 105118
    • 105321
    • 105184
    • 105245
    • 105339
    • 105240
Amount recalled
75 units

This recall covers 17 products

The agency filed one notice per product. You are reading one of them; the other 16 are below.

4 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

software syngo.CT VB20 in the installed base, with or without syngo.CT software versions VB20_SP1, SP2, SP3, or SP4, may result in workflow interruptions resulting in the delay in diagnosis, the necessity for patient rescans, and/or the need for additional contrast media may occur

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

Notice updated Jan 16, 2024 · Data as of Sep 19, 6:55 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.