Artis Q floor with software VD12- angiography systems recall
Artis Q floor with software VD12- angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number…
Why was Artis Q floor with software VD12- angiography systems recalled?
If SID (source-to-image distance) lift movement is activated and x-ray shall be released simultaneously; x-ray is not possible and the message No x-ray, try again is displayed, may result in a short delay in procedure
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?
Serial Numbers: Serial 104007 104016 104005 104027 104012 104025 104013 132500 Expanded Recall 11/15/21: 104029 104020
- Product
- Artis Q floor with software VD12- angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number…
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 8 units
- Distribution
- US Nationwide Distribution
- Recall date
- December 1, 2021
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)