FDA Device recall Z-2547-2019
IntelliVue 1.4 GHz Remote Antenna Used with Philips MX4O Monitors-The affected product is a 74 foot (22.6m) combined coax and unshielded tw…
- FDA Device
- Class II
- terminated
- Published 2019-09-25
On 2019-09-25 the FDA classified a Class II recall of IntelliVue 1.4 GHz Remote Antenna Used with Philips MX4O Monitors-The affected product is a 74 foot (22.6m) combined coax and unshielded tw… by Philips North America, citing remote Antenna Cable Used with Philips MX4O Monitors Does Not Have the Required Rating for Some Installations.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2547-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-08-23 |
| Published | 2019-09-25 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Philips North America |
| Distribution | US |
Product
IntelliVue 1.4 GHz Remote Antenna Used with Philips MX4O Monitors-The affected product is a 74 foot (22.6m) combined coax and unshielded twisted pair data cable bundle and is a component of the Philips Remote Antenna (PN 867151). The Remote Antenna is used with IntelliVue MX40 Patient Worn Monitors in the USA, to extend the coverage area of a Core Access Point for the wireless Smart-hopping system.
Reason
Remote Antenna Cable Used with Philips MX4O Monitors Does Not Have the Required Rating for Some Installations
Identifiers
| code_info | All Remote Antennas (PN 867151) shipped since May 2019 with marked "CM" rated coax data cable. Serial Numbers: DK82…All Remote Antennas (PN 867151) shipped since May 2019 with marked "CM" rated coax data cable. Serial Numbers: DK82001096 DK82000314 DK82000358 DK82000457 DK82000465 DK82000610 DK82000650 DK82000747 DK82000773 DK82000939 DK82001008 DK82001074 DK82001083 DK74900244 DK74900242 DK82000679 DK82000946 DK82000970 DK82000971 DK82000974 DK82001114 DK82001124 DK82001130 DK82001131 DK82001132 DK82001174 DK82001218 DK82001311 DK82101505 DK82101533 DK82101566 DK82101911 DK82102050 DK82102053 DK82102273 DK82000975 DK82000980 DK82000991 DK82000999 DK82001000 DK82001021 DK82001111 DK82001297 DK82001301 DK82001310 DK82101609 DK82101824 DK82101910 DK82102278 DK74900162 DK74900164 DK74900167 DK74900180 DK74900236 DK74900268 DK74900269 DK74900278 DK74900288 DK74900290 DK74900300 DK74900303 DK82000778 DK82000782 DK82000795 DK82000603 DK82000635 DK82000719 DK82000828 DK82000852 DK82000853 DK82000898 DK74900182 DK74900212 DK7490023 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2547-2019%22
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