Siemens Medical Solutions USA, Inc 2026-02-04 Health serious FDA
Health · FDA · Recall #FDA-Z-1174-2026
Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R; Siemens Material Number… Recall
Issued February 4, 2026 · Siemens Medical Solutions USA, Inc
In February 2026, Siemens Medical Solutions USA, Inc recalled the Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R; Siemens Material Number…, 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
Ortho images acquired with preset automatic horizontal flip are not flipped and when acquiring single images, there is the possibility that an image of a previous patient may be processed.
What you should do
- 1 Stop using Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R; Siemens Material Number… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Siemens Medical Solutions USA, Inc to arrange your voluntary. See the official notice below for contact details.
- 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
- February 4, 2026
- Units affected
- Not reported
- Sold at
- Worldwide - US Nationwide distribution in the states of AK, CA, IL, MN, NY, OR, VA, WI and the countries of Austria, Belgium, Denmark, Franc
- Recall number
- FDA-Z-1174-2026
- 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 356th Health recall we've logged in 2026.