Reported Jul 31, 2019 · Terminated

Artis zee floor, Model Number 10094135

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?

  • Artis zee floor, Model Number 10094135
Lot codes and dates
  • Serial Numbers

    170 of 170 codes

    • 135944
    • 135746
    • 135120
    • 135322
    • 135757
    • 136513
    • 136562
    • 135914
    • 135102
    • 136042
    • 135927
    • 135986
    • 135935
    • 135953
    • 135841
    • 135200
    • 135201
    • 135279
    • 135169
    • 135879
    • 135229
    • 135157
    • 136113
    • 135990
    • 136077
    • 136103
    • 135862
    • 135235
    • 135117
    • 135358
    • 135920
    • 136168
    • 135148
    • 135366
    • 136568
    • 135843
    • 135111
    • 135112
    • 135779
    • 136224
    • 135137
    • 136607
    • 136579
    • 135309
    • 124007
    • 124015
    • 136280
    • 136286
    • 135109
    • 135413
    • 135144
    • 135145
    • 136362
    • 135404
    • 136318
    • 136234
    • 135151
    • 135421
    • 135264
    • 135199
Amount recalled
170

This recall covers 23 products

The agency filed one notice per product. You are reading one of them; the other 22 are below.

10 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.

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 Sep 18, 2020 · Data as of Sep 19, 6:18 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.