Reported May 29, 2024 · Ongoing

Ingenia 3.0T- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device.…

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?

  • Ingenia 3.0T- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device
  • Model Number (REF)(1) 782103 (2) 781377 (3) 781342
Lot codes and dates
  • UDI-DI
    • (1) 782103 (01)00884838098299(21)
    • (2) 781377 (01)00884838009813(21)
    • (3) 781342 (01)00884838055339(21)
  • Serial NumbersSerial Number

    1,516 of 1,516 codes

    • 85106
    • 71011
    • 71152
    • 71403
    • 71433
    • 71526
    • 71710
    • 71812
    • 71817
    • 71101
    • 71168
    • 71178
    • 71179
    • 71214
    • 71252
    • 71309
    • 71313
    • 71328
    • 71342
    • 71419
    • 71453
    • 71550
    • 71551
    • 71555
    • 71557
    • 71674
    • 71693
    • 71733
    • 71859
    • 71949
    • 71993
    • 71994
    • 85036
    • 85045
    • 85155
    • 71266
    • 71311
    • 71345
    • 71392
    • 71395
    • 71628
    • 71723
    • 85393
    • 71216
    • 71651
    • 85208
    • 71163
    • 71408
    • 71493
    • 71499
    • 71541
    • 71668
    • 71729
    • 71771
    • 71602
    • 71260
    • 71276
    • 71324
    • 71800
    • 71726
Amount recalled
1517 units

This recall covers 32 products

The agency filed one notice per product. You are reading one of them; the other 31 are below.

19 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's technical room, resulting in Smoke and/or fire

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

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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, 7:35 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.