Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SmartPath to dStream for XR and 3.0T Model Numbers (REF): (1) 781270 Recalled by Philips North America Due to The potential for component failures in the Gradient...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Philips North America directly.
Affected Products
SmartPath to dStream for XR and 3.0T Model Numbers (REF): (1) 781270, (2) 782113, (3) 782129;
Quantity: 294 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips North America
Philips North America has 107 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report