FDAOctober 12, 2021device

Artis pheno with software VE20C- diagnostic imaging angiography system Model: 10849000

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

The hazard

Four potential software issues with Artis pheno and Artis icono systems with software VE20C: 1. Updated calibration data not saved with measurement after scene+/-; 2. No x-ray possible, system shutdown/restart might be required during intervention; 3. Corrupted Image during Roadmap; 4. Unintended shutdown of Imaging System with UPS (Uninterruptable Power Supply) option

What to do

FDA enforcement status: Terminated

Brands named

siemens medical solutionssiemenssiemens medical

UPCs

04056869046877

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 pheno with software VE20C- diagnostic imaging angiography system Model: 10849000 — Recall Details · AllClear