Philips North America 2025-08-06 Health serious FDA
Health · FDA · Recall #FDA-Z-2211-2025
Ingenia Elition X Model Numbers (REF): (1) 781358, (2) 782107, (3) 782119, (4) 782136,… Recall
Issued August 6, 2025 · Philips North America
In August 2025, Philips North America recalled the Ingenia Elition X Model Numbers (REF): (1) 781358, (2) 782107, (3) 782119, (4) 782136,…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
The potential for component failures in the Gradient Coil of the affected MR systems may act as a heat source with a potential to produce smoke and/or fire.
What you should do
- 1 Stop using Ingenia Elition X Model Numbers (REF): (1) 781358, (2) 782107, (3) 782119, (4) 782136,… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Philips North America 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
- Category
- Health
- Recall date
- August 6, 2025
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide and the countries of Albania, Algeria, Andorra, Angola, Argentina, Australia, Austria, Bahrain, Bangl
- Recall number
- FDA-Z-2211-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- Philips North America has 8 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.