FDADecember 30, 2019device

Integris Allura 9, system codes 722018 722021

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

The hazard

A capacitor inside the converter of the Velara X-ray generator may fail after a large number of surges in a short period of time. When this occurs, no image acquisition is possible.

What to do

FDA enforcement status: Terminated

Brands named

philips north americaphilipsphilips north

UPCs

722018722021

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 →