Artis icono biplane with software VE20C-diagnostic imaging angiography system Model: 11327600
Check against the official notice below — it lists the full affected range.
Siemens Medical Solutions USA, Inc. is recalling 72 Artis icono biplane diagnostic imaging angiography systems with software VE20C due to four potential software issues. These issues include: updated calibration data not being saved with measurements after scene adjustments, systems becoming unable to produce x-rays and potentially requiring shutdown and restart during interventions, corrupted images during roadmap procedures, and unintended shutdowns of the imaging system in units with uninterruptible power supply options. The affected systems were distributed nationwide and can be identified by their serial numbers, which are listed in the recall notice.
The recall notice does not specify a remedy or corrective action that affected consumers should take.
Written by software from the official notice below. Not reviewed by a lawyer.
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
Reason for recall: 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 Distribution: US Nationwide distribution. Quantity: 72 units Lot/code info: Serial Numbers: 180062 180318 180054 180019 180065 180057 180041 180317 180034 180072 180349 180060 180337 180070 180048 180083 180369 180370 180345 180315 180343 180080 180301 180305 180067 180330 180040 180360 180333 180029 180352 180336 180316 180068 180363 180084 180334 180018 180350 180354 180046 180047 180335 180085 180035 180339 180357 180358 180361 180362 180081 180331 180021 180342 180321 180309 180356 180368 180341 180323 180329 180043 180049 180077 180086 180053 180055 180015 180014 180066 180082 180037 UDI: 04056869063317 Expanded Recall 12/20/21 S/N: 180056
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.