FDAClass IIMarch 5, 2014

Siemens Artis zee Ceiling Systems. Angiographic x-ray recall

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

Why was Siemens Artis zee Ceiling Systems. Angiographic x-ray recalled?

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.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Artis zee Ceiling systems serial numbers from 146352 to 147617

Product
Siemens Artis zee Ceiling Systems. Angiographic x-ray system.
Recalling firm
Siemens Medical Solutions USA, Inc
Quantity
284
Distribution
Nationwide Distribution.
Recall date
March 5, 2014
Classification
Class II
Status
Terminated
Agency
FDA (device)
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