Reported Nov 29, 2023 · Ongoing

SmartPath to dStream for 1.5T

Philips North America LLC

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 Llc · 222 Jacobs St · Cambridge, MA · 02141-2289

Is this the product you have?

  • SmartPath to dStream for 1.5T
Lot codes and dates
  • Product No. 781260 & 782112
  • UDI-DI

    238 of 238 codes

    • (01)00884838095076(21)5447
    • (01)00884838095076(21)5463
    • (01)00884838095076(21)5479
    • (01)00884838095076(21)5490
    • (01)00884838095076(21)5537
    • (01)00884838095076(21)5546
    • (01)00884838095076(21)8012
    • (01)00884838095076(21)8025
    • (01)00884838095076(21)8054
    • (01)00884838095076(21)8086
    • (01)00884838095076(21)8087
    • (01)00884838095076(21)8091
    • (01)00884838095076(21)8092
    • (01)00884838095076(21)8110
    • (01)00884838095076(21)8118
    • (01)00884838095076(21)8178
    • (01)00884838095076(21)8260
    • (01)00884838095076(21)8311
    • (01)00884838095076(21)8318
    • (01)00884838095076(21)8365
    • (01)00884838095076(21)8378
    • (01)00884838095076(21)8387
    • (01)00884838095076(21)8392
    • (01)00884838095076(21)8395
    • (01)00884838095076(21)8427
    • (01)00884838095076(21)8554
    • (01)00884838095076(21)8566
    • (01)00884838095076(21)8578
    • (01)00884838095076(21)8611
    • (01)00884838095076(21)8616
    • (01)00884838095076(21)8639
    • (01)00884838095076(21)8642
    • (01)00884838095076(21)8667
    • (01)00884838095076(21)8706
    • (01)00884838095076(21)8713
    • (01)00884838095076(21)8746
    • (01)00884838095076(21)8750
    • (01)00884838095076(21)8752
    • (01)00884838095076(21)8779
    • (01)00884838095076(21)8783
    • (01)00884838095076(21)8786
    • (01)00884838095076(21)8831
    • (01)00884838095076(21)8840
    • (01)00884838095076(21)8851
    • (01)00884838095076(21)8857
    • (01)00884838095076(21)8884
    • (01)00884838095076(21)8895
    • (01)00884838095076(21)8896
    • (01)00884838095076(21)8923
    • (01)00884838095076(21)8942
    • (01)00884838095076(21)8948
    • (01)00884838095076(21)9004
    • (01)00884838095076(21)9013
    • (01)00884838095076(21)10029
    • (01)00884838095076(21)10044
    • (01)00884838095076(21)10075
    • (01)00884838095076(21)10079
    • (01)00884838095076(21)10130
    • (01)00884838095076(21)10151
    • (01)00884838095076(21)10164
Amount recalled
119 units

This recall covers 7 products

The agency filed one notice per product. You are reading one of them; the other 6 are below.

Where it was sold

  • Nationwide
  • PR

Why it was recalled

Potential component failure in the Gradient Coil could product smoke and/or fire.

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

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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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, 7:43 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.