Philips North America Llc 2025-07-02 Health serious FDA
Health · FDA · Recall #FDA-Z-2034-2025
Spectral CT. Computed tomography X-ray system. Recall
Issued July 2, 2025 · Philips North America Llc
In July 2025, Philips North America Llc recalled the Spectral CT. Computed tomography X-ray system., 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
Devices with affected software may experience two unintended motion issues that may lead to contact between the Gantry or table with the operator or patient, along with additional software issues that affect CT performance.
What you should do
- 1 Stop using Spectral CT. Computed tomography X-ray system. right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Philips North America Llc 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
- Philips North America Llc
- Category
- Health
- Recall date
- July 2, 2025
- Units affected
- Not reported
- Sold at
- Domestic: AZ, CA, CO, FL, GA, HI, IN, KY, MA, MD, MN, NY, OH, OR, PA, TX, VT, WA, WV; Foreign: Australia, Austria, Belgium, China, Czech Rep
- Recall number
- FDA-Z-2034-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- Philips North America Llc has 34 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.