FDADecember 12, 2025device

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

Official recall recorded by the U.S. Food & Drug Administration.

The 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.

What to do

FDA enforcement status: Ongoing

Brands named

philips north americaphilipsphilips north

UPCs

00884838099876

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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