FDAFDA · Food and drugs·Recall number Z-1309-2014
Artis Zee Angiographic x-ray systems.
Published April 9, 2014 · Recall initiated: February 7, 2014
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
An inappropriate cable connection was assembled for certain Artis zee systems. which may cause a system failure and possibly lead to a restricted maneuverability of the gantry system.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Siemens Medical Solutions USA, Inc
- Distributor
- MN, WI, PA, MI, AL, OH, NC, AR, and NJ.
- Lot
- Model numbers: 10094135, 10094137, 10094139, 10094141, 10280959.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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