FDAMay 2, 2024device

Philips Interventional Hemodynamic Application R.1.2X, R.1.3.0, R1.2.1. Software that enables invasive investigation of cardiac and vascular diseases.

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

The hazard

Potential for pressure wave data synchronization from two devices may not be correct.

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

UPCs

0088483810008400884838101180

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 →