Data Foundry

Medical device recalls 2019

IntelliVue 1 — Class II medical device recall Z-2547-2019

Terminated recall by Philips North America, LLC, reported 2019-09-25, distributed nationwide. Remote Antenna Cable Used with Philips MX4O Monitors Does Not Have the Required Rating for Some Installations

Recall numberZ-2547-2019
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmPhilips North America, LLC, Andover, MA, United States
Recall initiated2019-08-23
Classified2019-09-19
Reported by FDA2019-09-25
Terminated2024-01-03
DistributedNationwide (US)
Quantity1,790 units
Serial numbersDK74900162, DK74900164, DK74900165, DK74900167, DK74900168, DK74900169, DK74900170, DK74900171, DK74900173, DK74900175, DK74900176, DK74900177, DK74900178, DK74900180, DK74900182, DK74900183, DK74900185, DK74900186, DK74900200, DK74900201, DK74900202, DK74900207, DK74900210, DK74900212, DK74900217 and 475 more

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 for recall

Remote Antenna Cable Used with Philips MX4O Monitors Does Not Have the Required Rating for Some Installations

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2547-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.