FDADecember 19, 2014device

Philips IntelliVue Information Center iX (release A.00, A.01, and A.02) are impacted by this issue: 866023 IntelliVue Info Center iX 866024 PIIC iX Upgrade 866117 PIIC Classic Upgrade The intended use of the Information Center Software is to display physiologic waves, parameters, and trends, form...

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

The hazard

Sp02 and/or Non Invasive Blood Pressure (NBP) alarms may become disabled without visual notification

What to do

FDA enforcement status: Terminated

Brands named

philips medical systemsphilipsphilips medical

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 →