AllClear
PricingSign in
FDAFebruary 11, 2022device

CombiDiagnost R90 1.0 (709030)

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

The hazard

While performing a fluoroscopy examination, there is a potential that the Radio Fluoroscopy (RF) viewer will also display a previous patient's radiography images. If the issue occurs, there will be differences in image content, image format and image size.

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systemsphilipsphilips medical

UPCs

00884838076747

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 →
CombiDiagnost R90 1.0 (709030) — Recall Details · AllClear