Artis Q recall
Artis Q, Angiographic x-ray system Product Usage: The Artis systems are a family of dedicated angiography systems developed for single and biplane…
Why was Artis Q recalled?
The possibility exists that the semi-automatic focus switch may not work as intended when pressing the footswitch multiple times.
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: 10848280, 10848281, 10848282, 10848283, 10848353, 10848354, 10848355
- Product
- Artis Q, Angiographic x-ray system Product Usage: The Artis systems are a family of dedicated angiography systems developed for single and biplane…
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 4,657 systems (worldwide)
- Distribution
- US Nationwide Distribution.
- Recall date
- November 23, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)