Reported Aug 6, 2025 · Ongoing

Ingenia 1.5T Model Numbers (REF): (1) 781315, (2) 718641, (3) 781396, (4) 782101, (5) 782115, (6) 782140;

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?

  • Ingenia 1.5T
  • Model Numbers (REF)
    • (1) 781315
    • (2) 718641
    • (3) 781396
    • (4) 782101
    • (5) 782115
    • (6) 782140
Lot codes and dates
  • Model Numbers (REF)
    • (1) 781315
    • (2) 718641
    • (3) 781396
    • (4) 782101
    • (5) 782115
    • (6) 782140
  • UDI-DI
    • (1) 00884838099715
    • (2) 00884838055322
    • (3) 00884838009820
    • (4) 00884838098275
    • (5) 00884838099043
    • (6) 00884838108646
  • Serial Numbers

    2,279 of 2,279 codes

    • (1) 61000
    • 61001
    • 61002
    • 61003
    • 61004
    • 61005
    • 61006
    • 61007
    • 61008
    • 61009
    • 61011
    • 61013
    • 61014
    • 61015
    • 61016
    • 61017
    • 61018
    • 61019
    • 61020
    • 61022
    • 61023
    • 61024
    • 61025
    • 61026
    • 61027
    • 61028
    • 61029
    • 61030
    • 61031
    • 61032
    • 61033
    • 61034
    • 61035
    • 61036
    • 61037
    • 61038
    • 61039
    • 61040
    • 61041
    • 61042
    • 61043
    • 61044
    • 61045
    • 61046
    • 61047
    • 61049
    • 61050
    • 61051
    • 61052
    • 61053
    • 61054
    • 61055
    • 61056
    • 61057
    • 61058
    • 61059
    • 61060
    • 61061
    • 61062
    • 61063
Amount recalled
2,279 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.

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, 4:08 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.