AllClear
PricingSign in
FDAFebruary 22, 2017device

ARTIS Q, Interventional Fluroscopic x-ray system

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

The hazard

In Artis systems with A100G generators, a component can be affected by aging which could result in the potential failure of a module in the high-voltage generator.

What to do

FDA enforcement status: Terminated

Brands named

siemens medical solutionssiemenssiemens 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 →
ARTIS Q, Interventional Fluroscopic x-ray system — Recall Details · AllClear