Reported Jun 7, 2017 · Terminated

NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383)

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?

  • NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383)
Lot codes and dates
  • System Serial Number

    2,715 of 2,715 codes

    • DE24702801
    • DE24702582
    • DE33103000
    • DE33103006
    • DE33104465
    • DE33104466
    • DE33104469
    • DE33104473
    • DE33104497
    • DE44306376
    • DE44305951
    • DE33105241
    • DE33105483
    • DE44306622
    • DE44306625
    • DE44306626
    • DE44306644
    • DE44306645
    • DE44306657
    • DE44306604
    • DE44306608
    • DE44306638
    • DE44306639
    • DE33103007
    • DE33103055
    • DE33103062
    • DE33103493
    • DE44307378
    • DE44307381
    • DE44307385
    • DE44307391
    • DE44307392
    • DE44307395
    • DE24702503
    • DE24702507
    • DE24702508
    • DE24702509
    • DE24702510
    • DE24702511
    • DE24702512
    • DE24702513
    • DE24702514
    • DE24702515
    • DE24702516
    • DE24702517
    • DE24702518
    • DE24702520
    • DE24702521
    • DE24702563
    • DE33104560
    • DE33104569
    • DE24702655
    • DE24702656
    • DE44305701
    • DE44305702
    • DE44305706
    • DE44305709
    • DE44305734
    • DE44305745
    • DE44305746
Amount recalled
9120 devices

Where it was sold

Why it was recalled

Manufacturing defect may cause localized heating, which may result in localized skin burn.

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.

Free recall alerts

Get alerted about new Philips Electronics North America Corporation recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jun 28, 2018 · Data as of Sep 19, 6:00 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.