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Recall Observatory FDA recall evidence

Device product

Siemens Artis zee Ceiling Systems. Angiographic x-ray system.

Z-1080-2014

December 16, 2013

Class II

Product summary

Firm
Siemens Medical Solutions USA, Inc
Event
Event 67175
Status
Terminated
Classification
Class II
Quantity
284
Official record key
device-enforcement:Z-1080-2014

Official wording

Reason: During the lifetime of Artis zee Ceiling systems, there is an increased wear due to potential sub-optimal cable guidance that can lead to cable damage.

Code information: Artis zee Ceiling systems serial numbers from 146352 to 147617

Distribution pattern: Nationwide Distribution.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    During the lifetime of Artis zee Ceiling systems, there is an increased wear due to potential sub-optimal cable guidance that can lead to cable damage.