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Philips North America Llc recalls Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor.
Recalled January 14, 2026 · FDA recall Z-1033-2026 · Philips North America
Hazard
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. · FDA Class II
Units
13,470 Units
Sold at
US Nationwide distribution.
Description
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.
Product
Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor.
Manufacturer(s)
Philips North America Llc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →