FDA recall Z-1033-2026

Product

Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor.

Reason for recall

It was found that the MX40 device could not reconnect to the PIC iX when moving between Radiohead and Trident 1.4 GHz access points if the signal strength changed quickly.

Distribution

US Nationwide distribution.

Key facts

Status

Ongoing

Initiation date

2025-12-12

Report date

2026-01-14

Voluntary/Mandated

Voluntary: Firm initiated

Location

Cambridge, MA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1033-2026