Reported Apr 25, 2018 · Terminated

Intera 1.5T; 1) Intera 1.5T Omni/Stellar Model 781104, 2) Intera 1.5T Power/Pulsar Model 781105, 3) Intera 1.5T…

Philips Electronics North America Corporation

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 Electronics North America Corporation · 3000 Minuteman Rd · Andover, MA · 01810-1032

Is this the product you have?

15 of 15 products

Products covered by this recall
Model / numberProduct as published
781104Intera 1.5T Omni/Stellar
781105Intera 1.5T Power/Pulsar
781106Intera 1.5T Master/Nova
781107Intera 1.5T Master CV
781108Intera 1.5T Explorer/ Nova Dual
781160Intera 1.5T IT
781170Intera 1.5T Pulsar
781171Intera 1.5T Achieva Pulsar
781172Intera 1.5T Achieva Nova
781174Intera 1.5T Achieva CV Nova
781174Intera 1.5T Achieva IT Nova
781176Intera 1.5T Achieva I/T Nova Dual
781195Intera 1.5T
781295Intera 1.5T Pulsar New , (Added 6/25/18)
Intera 1.5T Enterprise
Lot codes and dates
  • (Added 6/25/18):

    511 of 511 codes

    • 8920
    • 8590
    • 8368
    • 8210
    • 10049
    • 8277
    • 10039
    • 10087
    • 8302
    • 18629
    • 8050
    • 18749
    • 10777
    • 8699
    • 18554
    • 8250
    • 8073
    • 8540
    • 18050
    • 10691
    • 18784
    • 8056
    • 10198
    • 8244
    • 8583
    • 8889
    • 18079
    • 8408
    • 10031
    • 8052
    • 8899
    • 8234
    • 10137
    • 18974
    • 10014
    • 8612
    • 8916
    • 10133
    • 8928
    • 10789
    • 18966
    • 10118
    • 10195
    • 8009
    • 8846
    • 8668
    • 8797
    • 10092
    • 10732
    • 8233
    • 18034
    • 8003
    • 18723
    • 8418
    • 8934
    • 10111
    • 8536
    • 8268
    • 8462
    • 10727
Amount recalled
8,205 units in total

This recall covers 13 products

The agency filed one notice per product. You are reading one of them; the other 12 are below.

Where it was sold

  • Nationwide
  • GA

Why it was recalled

Potential risk for helium gas inside the MR examination room during a magnet quench

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

Notice updated Apr 10, 2020 · Data as of Sep 19, 4:48 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.