Reported Aug 16, 2023 · Ongoing

Ingenia Elition S Magnetic Resonance (MR) system, Product Numbers 781357 and 782106

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 Elition S Magnetic Resonance (MR) system, Product Numbers 781357 and 782106
Lot codes and dates
  • Product Number781357:
  • UDI-DI00884838088108
  • Serial Numbers

    75 of 75 codes

    • 46119
    • 46111
    • 46109
    • 46107
    • 46104
    • 46101
    • 46097
    • 46095
    • 4609446093
    • 46092
    • 46089
    • 46088
    • 46086
    • 46085
    • 46084
    • 46083
    • 46082
    • 46081
    • 46078
    • 46077
    • 46076
    • 46075
    • 46071
    • 46069
    • 46068
    • 46067
    • 4606646065
    • 46061
    • 46060
    • 46059
    • 46058
    • 46057
    • 46055
    • 46054
    • 46053
    • 46052
    • 46050
    • 46049
    • 46048
    • 46046
    • 46045
    • 46044
    • 46042
    • 46041
    • 4603946037
    • 46036
    • 46034
    • 46033
    • 46032
    • 46031
    • 46030
    • 46029
    • 46027
    • 46026
    • 46025
    • 46024
    • 46023
    • 46021
    • 46020
    • 46019
  • Product Number 782106UDI-DI:00884838098329
  • Serial Numbers
    • 61017
    • 61010
    • 46324
    • 46315
    • 46311
    • 46310
    • 46304
    • 46289
    • 46286
    • 46285
    • 46282
    • 46270
    • 46269
    • 4626846265
    • 46258
    • 46252
    • 46249
    • 46247
    • 46243
    • 46241
    • 46240
    • 46239
    • 46237
    • 46235
    • 46234
    • 46233
    • 46231
    • 46228
    • 46226
    • 46225
    • 46224
    • 4622246220
    • 46219
    • 46218
    • 46217
    • 46215
    • 46214
    • 46213
    • 46212
    • 46211
    • 46209
    • 46208
    • 46207
    • 46206
    • 46205
    • 46204
    • 46203
    • 46202
    • 46201
    • 4620046242
    • 46245
    • 46263
    • 46305
    • 46264
    • 46281
Amount recalled
601 Total

This recall covers 6 products

The agency filed one notice per product. You are reading one of them; the other 5 are below.

Where it was sold

  • Nationwide

Why it was recalled

During installation of the SmokeDetector Interlock, a connecting cable, between the SmokeDetector Interlock and the host PC, may not have been properly installed. This connection is used for service diagnostics and does not impact the functionality of the system and/or the SmokeDetector Interlock system.

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, 6:55 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.