NMT Patient Cable
Medical device recall Z-2175-2017. Published in FDA’s Enforcement Report on Jun 7, 2017.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Jun 7, 2017. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- 31 states named in where it went
- 9120 devices how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
Manufacturing defect may cause localized heating, which may result in localized skin burn.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383)
9120 devices, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
System Serial Number: DE24702801 DE24702582 DE33103000 DE33103006 DE33104465 DE33104466 DE33104469 DE33104473 DE33104497 DE44306376 DE44305951 DE33105241 DE33105483 DE44306622 DE44306625 DE44306626 DE44306644 DE44306645 DE44306657…
Every code shown here, 1,991 characters
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 DE33104871 DE33104881 DE33104878 DE33104879 DE44307338 DE44307311 DE44307327 DE44307330 DE44306896 DE33105420 DE33105556 DE33105558 DE44307636 DE44307609 DE44307610 DE44307611 DE44307612 DE44307616 DE44307617 DE44307619 DE44307620 DE44307621 DE44307628 DE44307635 DE44307637 DE22801752 DE44305695 DE44305696 DE44305697 DE44305707 DE44305710 DE44305711 DE44305712 DE44305717 DE44305728 DE44305729 DE33103729 DE33103731 DE33103735 DE33103737 DE33103738 DE33103739 DE33103742 DE33103749 DE33103989 DE33103999 DE33103896 DE33105418 DE44306377 DE44306384 DE44306385 DE44306388 DE44306389 DE44306391 DE44306394 DE44306395 DE44306396 DE44306397 DE44306399 DE44306400 DE44306401 DE44306402 DE44306403 DE44306404 DE44306405 DE44306406 DE44306407 DE44306408 DE44306411 DE44306412 DE44306413 DE44306175 DE33103068 DE33103079 DE33103090 DE33103094 DE33103017 DE33103019 DE33103020 DE33103060 DE33103066 DE33103067 DE33103069 DE33103071 DE33103072 DE33103080 DE33103083 DE33103086 DE33103087 DE33103088 DE33103089 DE33103075 DE33103093 DE33103102 DE33102973 DE33102974 DE33102969 DE33102978…
FDA’s list runs to 67,073 characters. The first part is shown; the rest is on FDA’s record.
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
US: 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 OUS: Algeria Argentina Australia Austria Bahrain Belarus Belgium Bolivia Brazil Canada Chile China Colombia Costa Rica Denmark Dominican Rep Egypt Finland France Germany Hong Kong Hungary Iceland India Indonesia Ireland Israel Italy Japan Latvia Lebanon Libya Lithuania Luxembourg Malaysia Mexico Mongolia Netherlands New Zealand Norway Oman Pakistan Peru Philippines Poland Portugal Qatar Romania Russia Russian Fed. Saudi Arabia Singapore Slovenia South Africa South Korea Spain Sweden Switzerland Taiwan Thailand Tunisia Turkey Ukraine United Kingdom Utd.Arab.Emir.
The states and territories these words name
31 states and territories.
Every one of them
- Alaska
- Arizona
- California
- Colorado
- Florida
- Hawaii
- Iowa
- Illinois
- Indiana
- Kentucky
- Massachusetts
- Maryland
- Michigan
- Minnesota
- Missouri
- Mississippi
- North Carolina
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oregon
- Pennsylvania
- Texas
- Virginia
- Washington
- Wisconsin
- West Virginia
The words say it went outside the United States too.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on May 4, 2017.
- FDA classified it on May 31, 2017.
- FDA’s Enforcement Report published it on Jun 7, 2017.
- FDA terminated it on Jun 28, 2018.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Philips Electronics North America Corporation, of Andover, MA.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- FDA’s list of codes runs to 67,073 characters; the first part is shown here, and the rest is on FDA’s record.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
-
U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.