Reported Feb 3, 2021 · Terminated

TRx4841A 1.4 GHz IntelliVue Tele TRX, Model Number 862439; Includes System Codes 453564007261, 453564007271,…

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 · 3000 Minuteman Rd · Andover, MA · 01810-1032

Is this the product you have?

    • TRx4841A 1.4 GHz IntelliVue Tele TRX
    • Model Number 862439
    • Includes System Codes 453564007261
    • 453564007271
    • 453564007281
    • 989803196951
Lot codes and dates
  • Serial Numbers

    2,358 of 2,358 codes

    • US94348760
    • US53404426
    • US11479851
    • US53404552
    • US53404773
    • US65112716
    • US61307506
    • US63409602
    • US65113980
    • US11482453
    • US44801180
    • US53404420
    • US00552837
    • US00554294
    • US71218273
    • US53402710
    • US53402748
    • US53402489
    • US44800249
    • US73729592
    • US53404994
    • US44800361
    • US53406037
    • US53404431
    • US00554876
    • US00554879
    • US73728988
    • US52402192
    • US65112718
    • US65113706
    • US65112932
    • US73731015
    • US71216309
    • US63411735
    • US44801179
    • US53403403
    • US71217875
    • US03862052
    • US61306876
    • US53405461
    • US02656890
    • US53403885
    • US50901456
    • US53403109
    • US53405111
    • US65112438
    • US44800332
    • US00550542
    • US00550535
    • US71217878
    • US50901335
    • US71217882
    • US83233987
    • US53403371
    • US00551365
    • US83231550
    • US53405148
    • US00550937
    • US94348947
    • US11470201
Amount recalled
81,626

This recall covers 2 products

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

Where it was sold

  • Nationwide

Why it was recalled

The ECG signal from patients being monitored using a Philips TRx4841A and TRx4851A Telemetry Transceiver may not be properly analyzed when it is used with a Philips Patient Information Center iX Release C.02.xx or C.03.01. If this occurs, the Information Center will not display a heart rate or generate, display or annunciate any heart rate or arrhythmia alarms.

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 Feb 11, 2021 · Data as of Sep 19, 4:50 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.