Artis zee and Artis zeego systems. x-ray recall: Software Issue
Artis zee and Artis zeego systems. x-ray, angiographic system
Why was Artis zee and Artis zeego systems. x-ray recalled?
There is a potential problem with Artis zee and Artis zeego systems running software version VC21B and being used in conjunction with the Large Display, in that under certain circumstances, the release of radiation can become blocked unnecessarily.
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?
running software version VC21B 10094135, 10094137, 10094141, 10280959 with multiple serial numbers .
- Product
- Artis zee and Artis zeego systems. x-ray, angiographic system
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 206
- Distribution
- Nationwide Distribution
- Recall date
- October 1, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)