Recall Z-1033-2026— Philips North America Llc

Name: FDA recall Z-1033-2026
Creator: U.S. Food and Drug Administration
Published: 2025-12-12

Class II · Ongoing

Class II FDA medical device recall by Philips North America Llc, initiated 2025-12-12. FDA's recall record names no specific 510(k) clearance for this event. Product: Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor.. Reason: 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..

Recalling firm: Philips North America Llc
Classification: Class II
Status: Ongoing
Initiated: 2025-12-12
Firm location: Cambridge, MA, United States

Product description

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.