Reported Apr 27, 2022 · Ongoing

Artis Q ceiling, Model Number 10848281

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 Q ceiling, Model Number 10848281
Lot codes and dates
  • UDI4056869009988
  • Serial Numbers

    404 of 404 codes

    • 109130
    • 109490
    • 109552
    • 110088
    • 110059
    • 110103
    • 133503
    • 109799
    • 110035
    • 109642
    • 109892
    • 109135
    • 109569
    • 109123
    • 110046
    • 109400
    • 110005
    • 109812
    • 109727
    • 109210
    • 109628
    • 110058
    • 109931
    • 110056
    • 109080
    • 109610
    • 110062
    • 109074
    • 109746
    • 109417
    • 109479
    • 109352
    • 109388
    • 109190
    • 109191
    • 109197
    • 109198
    • 109418
    • 109419
    • 109421
    • 133000
    • 133201
    • 109305
    • 109789
    • 109792
    • 109889
    • 109592
    • 109738
    • 109405
    • 109657
    • 109119
    • 109346
    • 109016
    • 109523
    • 109645
    • 109118
    • 109693
    • 109493
    • 110067
    • 109583
  • Additional Serial Numbers as of 10/4/23
    • 133504
    • 109145
    • 109211
    • 109350
    • 109461
    • 103053
    • 103040
    • 109308
    • 109416
    • 109457
    • 109225
    • 109222
    • 109224
    • 109320
Amount recalled
418 systems

This recall covers 18 products

The agency filed one notice per product. You are reading one of them; the other 17 are below.

5 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

If the coolant level in the cooling circuit drops below a certain level, this may result in a situation in which the X-ray tube is no longer sufficiently cooled and the system will display the message "TUBE HOT, have a break". Several minutes later the system will block X-ray to prevent further damage and display the message "NO XRAY: TUBE TOO HOT".

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, 5:34 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.