FDADecember 22, 2025device

Patient Information Center iX; Software Version Number: 4.5.0

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

The hazard

A recent software (SW) patch modifies Mobile Event Notification filter settings without providing any indication to the user when upgrading the system.

What to do

FDA enforcement status: Ongoing

Brands named

philips north americaphilipsphilips north

UPCs

00884838127074

Recall history

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

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →
Patient Information Center iX; Software Version Number: 4.5.0 — Recall Details · AllClear