FDAFDA · Food and drugs·Recall number Z-1080-2014
Siemens Artis zee Ceiling Systems. Angiographic x-ray system.
Published March 5, 2014 · Recall initiated: December 16, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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 to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Siemens Medical Solutions USA, Inc
- Distributor
- Nationwide Distribution.
- Lot
- Artis zee Ceiling systems serial numbers from 146352 to 147617
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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