Artis zee ceiling with software VD12-angiography recall
Artis zee ceiling with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model…
Why was Artis zee ceiling with software VD12-angiography 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 150002 150017 125700 150005 150023 150009 150015 150003 Expanded Recall 11/15/21: 147120 147119 150011
- Product
- Artis zee ceiling with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model…
- 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)