Reported Aug 6, 2025 · Ongoing

SmartPath to dStream for XR and 3.0T Model Numbers (REF): (1) 781270, (2) 782113, (3) 782129;

Philips North America

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Philips North America · 222 Jacobs St · Cambridge, MA · 02141-2296

Is this the product you have?

  • SmartPath to dStream for XR and 3.0T
  • Model Numbers (REF)
    • (1) 781270
    • (2) 782113
    • (3) 782129
Lot codes and dates
  • Model Numbers (REF)
    • (1) 781270
    • (2) 782113
    • (3) 782129
  • UDI-DI
    • (1) 00884838095083
    • (2) 00884838098909
    • (3) 00884838105805
  • Serial Numbers

    294 of 294 codes

    • (1) 17006
    • 17172
    • 17204
    • 17206
    • 17212
    • 17215
    • 17222
    • 17237
    • 17239
    • 17240
    • 17242
    • 17245
    • 17246
    • 17247
    • 17250
    • 17260
    • 17264
    • 17265
    • 17266
    • 17268
    • 17269
    • 17274
    • 17283
    • 17284
    • 17286
    • 17290
    • 17292
    • 17299
    • 17302
    • 17308
    • 17309
    • 17313
    • 17321
    • 17326
    • 17339
    • 17342
    • 17344
    • 17352
    • 17353
    • 17356
    • 17357
    • 17360
    • 17366
    • 17367
    • 17369
    • 17375
    • 17378
    • 17386
    • 17388
    • 17389
    • 17398
    • 17399
    • 17406
    • 17415
    • 17416
    • 17425
    • 17428
    • 17429
    • 17434
    • 17436
Amount recalled
294 units

This recall covers 19 products

The agency filed one notice per product. You are reading one of them; the other 18 are below.

6 more are in the archive.

Where it was sold

  • Nationwide
  • GA

Why it was 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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:19 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.