Artis Zee Angiographic x-ray systems recall
Artis Zee Angiographic x-ray systems.
Why was Artis Zee Angiographic x-ray systems recalled?
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 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?
Model numbers: 10094135, 10094137, 10094139, 10094141, 10280959.
- Product
- Artis Zee Angiographic x-ray systems.
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 9
- Distribution
- MN, WI, PA, MI, AL, OH, NC, AR, and NJ.
- Recall date
- April 9, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)