Skip to content
Recall Observatory FDA recall evidence

Device product

ARTIS zee and zeego x-ray, angiographic system with Software Artis VC20x/VC21A that have Patch 7 and a 3D and DSA license installed. Angiographic x-ray system

Z-1782-2013

June 26, 2013

Class II

Product summary

Firm
Siemens Medical Solutions USA, Inc
Event
Event 65651
Status
Terminated
Classification
Class II
Quantity
29
Official record key
device-enforcement:Z-1782-2013

Official wording

Reason: Siemens issued a customer safety advisory notice and field safety corrective action for a potential issue on Artis systems with Artis VC20x/VC21A that have Patch 7 and a 3D and DSA license installed. The issue affects-DSA rotational acquisition. The restriction is related to any rotational 3D-acquisition program with real-time subtraction (e.g. 3D DSA). During the fill phase of the rotational aqui

Code information: Model numbers: 10094137, 10094139, 10094141, 10280959

Distribution pattern: Nationwide Distribution and Puerto Rico

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Siemens issued a customer safety advisory notice and field safety corrective action for a potential issue on Artis systems with Artis VC20x/VC21A that have Patch 7 and a 3D and DSA license installed. The issue affects-DSA rotational acquisition. The restriction is related to any rotational 3D-acquisition program with real-time subtraction (e.g. 3D DSA). During the fill phase of the rotational aqui