Class II

Medical Device Recall: Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor.

Philips North America Llc · December 12, 2025

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.

States Affected

NATIONWIDE

Quantity Affected

13,470 Units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1033-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.