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Serious recall: Injury is possible or has been reported. Take action promptly.

Siemens Medical Solutions USA, Inc 2023-01-25 Health serious FDA
Health · FDA · Recall #FDA-Z-0956-2023

ARTIS pheno, ARTIS icono biplane, and ARTIS icono floor Recall

Issued January 25, 2023 · Siemens Medical Solutions USA, Inc

In January 2023, Siemens Medical Solutions USA, Inc recalled the ARTIS pheno, ARTIS icono biplane, and ARTIS icono floor, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Mechanical connection between the tabletop and table base may be lost.

What you should do

  1. 1 Stop using ARTIS pheno, ARTIS icono biplane, and ARTIS icono floor right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Siemens Medical Solutions USA, Inc to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Siemens Medical Solutions USA, Inc
Category
Health
Recall date
January 25, 2023
Units affected
Not reported
Sold at
Worldwide distribution - US Nationwide and the countries of Armenia, Australia, Austria, Belgium, Bulgaria, Canada, Chile, China, Colombia,
Recall number
FDA-Z-0956-2023
Made in
United States
Issuing agency
FDA

In context

  • Siemens Medical Solutions USA, Inc has 17 recalls in our database, including 2 rated Critical.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 903rd Health recall we've logged in 2023.
Read the official FDA notice

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