FDA Device recall Z-0020-2025
IntelliVue Patient Monitor MX400/MX450/MX500/MX550 with software version P.01.01 and ordered with Option CP2 are affected as follows: 1) In…
- FDA Device
- Class II
- ongoing
- Published 2024-10-16
On 2024-10-16 the FDA classified a Class II recall of IntelliVue Patient Monitor MX400/MX450/MX500/MX550 with software version P.01.01 and ordered with Option CP2 are affected as follows: 1) In… by Philips North America, citing 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 CP….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0020-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-06-14 |
| Published | 2024-10-16 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Philips North America |
| Distribution | n/a |
Product
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.
Reason
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.
Identifiers
| code_info | UDI-DI: (01)00884838038769(21); (01)00884838038776(21); (01)00884838038783(21 Serial Numbers: DE7580BB1Y DE7580BB1Z DE…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 DE7 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0020-2025%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.