IntelliVue Patient Monitor MX400/MX450/MX500/MX550 with software version P.01.01 and ordered with Option CP2…
Medical device recall Z-0020-2025. Published in FDA’s Enforcement Report on Oct 16, 2024.
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 Oct 16, 2024. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Ongoing its status, in FDA’s file
- Not named no state, in where it went
- 153 units OUS 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?
Devices with Option CP2 and initially programmed to software version P.01.01 were configured incorrectly at the factory. Therefore, Enhanced ECG Capabilities provided by Option CP2 were not enabled in these devices. Without Option C01 Full Arrhythmia, the device will not provide the yellow alarms for enhanced arrhythmia detection. This is a retrospectively reported recall from 6/14/23.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
IntelliVue Patient Monitor MX400/MX450/MX500/MX550 with software version P.01.01 and ordered with Option CP2 are affected as follows: 1) IntelliVue MX400 866060; 2) IntelliVue MX450 866062; 3) IntelliVue MX500 866064; 4) IntelliVue MX550 866066 Indicated for use by health care professionals whenever there is a need for monitoring the physiological parameters of patients.
153 units OUS, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
UDI-DI: (01)00884838038769(21); (01)00884838038776(21); (01)00884838038783(21 Serial Numbers: DE7580BB1Y DE7580BB1Z DE7580BB20 DE7580BB21 DE7580BB22 DE7580BB23 DE7580BB24 DE7580BB25 DE7580BC47 DE7580BC48 DE7580BC4L DE7580BC4M DE7580BC4N…
Every code shown here, 1,776 characters
UDI-DI: (01)00884838038769(21); (01)00884838038776(21); (01)00884838038783(21 Serial Numbers: DE7580BB1Y DE7580BB1Z DE7580BB20 DE7580BB21 DE7580BB22 DE7580BB23 DE7580BB24 DE7580BB25 DE7580BC47 DE7580BC48 DE7580BC4L DE7580BC4M DE7580BC4N DE7580BC4P DE7580BC4T DE7580BC4U DE7580BC5K DE7580BC5L DE7580BC5N DE7580BC5P DE7580BC5R DE7580BC5T DE7580BC5U DE7580BC5V DE7580BC68 DE7580BC69 DE7580BC6A DE7580BC6B DE7580BC6C DE7580BC6D DE7580BC6E DE7580BC6R DE7580BC6Z DE7580BC8R DE7580BCV4 DE7580BD4K DE7580BD4L DE7580BF3Z DE7580BFUL DE7580BFUM DE7580BFUN DE7580BFWY DE7580BJM2 DE7580BJM3 DE7580BJM4 DE7580BJM5 DE7580BJM6 DE7580BJM7 DE7580BJWV DE7580BJWW DE7580BJWY DE7580BJWZ DE7580BJY0 DE7580BJY1 DE7580BK55 DE7580BK56 DE7580BK75 DE7580BK76 DE7580BK77 DE7580BK78 DE7580BK79 DE7580BK7A DE7580BK7B DE7580BK7C DE7580BK7D DE7580BK7E DE7580BC3A DE7580BC3B DE7580BC3C DE7580BC3E DE7580BC3F DE7580BC3G DE7580BC3H DE7580BC3J DE7580BC3K DE7580BC3L DE7580BC3M DE7580BC3N DE7580BC3R DE7580BC3T DE7580BC3U DE7580BC3V DE7580BC3W DE7580BC3Y DE7580BC3Z DE7580BC40 DE7580BC41 DE7580BC42 DE7580BC43 DE7580BC75 DE7580BC79 DE7580BCY8 DE7580BCY9 DE7580BCYA DE7580BCYB DE7580BCYD DE7580BCYE DE7580BCYF DE7580BCYG DE7580BCYK DE7580BCYL DE7580BDE4 DE7580BDE5 DE7580BDE6 DE7580BDE7 DE7580BE0K DE7580BE0L DE7580BEWY DE7580BHZT DE7580BNKB DE7580BNKC DE7580BNKD DE7580BNKE DE7580BBBA DE7580BBUE DE7580BBUK DE7580BBUL DE7580BBUY DE7580BBUZ DE7580BBV0 DE7580BBV1 DE7580BBVC DE7580BBVD DE7580BBVE DE7580BBVF DE7580BBVU DE7580BBVV DE7580BBVY DE7580BBW9 DE7580BBWA DE7580BBWB DE7580BBWC DE7580BBWP DE7580BBWR DE7580BBYR DE7580BC2E DE7580BC2F DE7580BC2G DE7580BC2H DE7580BC2M DE7580BC2N DE7580BC2P DE7580BC2R DE7580BC2T DE7580BC2U DE7580BC2V DE7580BC2W DE7580BC2Y DE7580BC2Z DE7580BFVB DE7580BK89 DE7580BK8A DE7580BK8B
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.
Foreign Only: Denmark France Germany Japan United Kingdom
These words name no state.
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?
Ongoing, in FDA’s file.
“A recall which is currently in progress.”
openFDA, on “On-Going”, 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 Jun 14, 2023.
- FDA classified it on Oct 4, 2024.
- FDA’s Enforcement Report published it on Oct 16, 2024.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Philips North America Llc, of Cambridge, 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.”
- 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
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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.