FDA Device recall Z-2175-2017

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

FDA Device
Class II
terminated
Published 2017-06-07

On 2017-06-07 the FDA classified a Class II recall of NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383) by Philips Electronics North America, citing manufacturing defect may cause localized heating, which may result in localized skin burn.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-2175-2017
Classification	Class II
Status	terminated
Initiated	2017-05-04
Published	2017-06-07
Last updated	2026-09-13 11:54 UTC
Company	Philips Electronics North America
Distribution	AK, AZ, CA, CO, FL, HI, IA, IL, IN, KY, MA, MD, MI, MN, MO, MS, NC, NE, NH, NJ, NM, NV, NY, OH, OR, PA, TX, VA, WA, WI, WV

Product

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

Reason

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

Identifiers

code_info	System Serial Number: DE24702801 DE24702582 DE33103000 DE33103006 DE33104465 DE33104466 DE33104469 DE33104473 D… System Serial Number: 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 DE44305748 DE44305751 DE24702492 DE33105536 DE44305884 DE33105413 DE33105416 DE33105432 DE44305788 DE24702254 DE24702257 DE24702262 DE24702265 DE33103146 DE33103147 DE33103154 DE33103144 DE33103577 DE33103457 DE33103458 DE33103912 DE3310

code_info

System Serial Number: DE24702801 DE24702582 DE33103000 DE33103006 DE33104465 DE33104466 DE33104469 DE33104473 D…

System Serial Number: 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 DE44305748 DE44305751 DE24702492 DE33105536 DE44305884 DE33105413 DE33105416 DE33105432 DE44305788 DE24702254 DE24702257 DE24702262 DE24702265 DE33103146 DE33103147 DE33103154 DE33103144 DE33103577 DE33103457 DE33103458 DE33103912 DE3310

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2175-2017%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.