Reported Jul 4, 2018 · Terminated

Artis zee ceiling, Material no. 10094137, for angiography and whole body radiographic/fluoroscopic procedures.

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 ceiling, Material no. 10094137, for angiography and whole body radiographic/fluoroscopic procedures.
Lot codes and dates
  • 73 of 73 codes

    • 147763
    • 147573
    • 147608
    • 147760
    • 147636
    • 147630
    • 147208
    • 147514
    • 147165
    • 147558
    • 147304
    • 146946
    • 147585
    • 147553
    • 147645
    • 147087
    • 147203
    • 147601
    • 147659
    • 147675
    • 147516
    • 147700
    • 147745
    • 147681
    • 147795
    • 147773
    • 147789
    • 147541
    • 147577
    • 147029
    • 147625
    • 147635
    • 146152
    • 147660
    • 147753
    • 147083
    • 146861
    • 147561
    • 147771
    • 147657
    • 147364
    • 147775
    • 147790
    • 147781
    • 147734
    • 146896
    • 147559
    • 147620
    • 147287
    • 147749
    • 147633
    • 147737
    • 147621
    • 147250
    • 147253
    • 147252
    • 147251
    • 147717
    • 147778
    • 147643
Amount recalled
73

This recall covers 13 products

The agency filed one notice per product. You are reading one of them; the other 12 are below.

Where it was sold

  • Nationwide
  • PR

Why it was recalled

After the Large Display returns from power save mode, it may not show an image, and stay black without showing an error message although X-ray is still possible. The problem does not occur during an ongoing procedure. If the problem occurs, the system cannot be operated normally. It may be necessary to cancel or restart the treatment or transfer the patient to an alternate or another system.

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 May 16, 2019 · Data as of Sep 19, 6:16 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.