AXIOM Artis dFA recall
AXIOM Artis dFA, Model Number 7555373
Why was AXIOM Artis dFA recalled?
A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going 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: 50063 50059 50006 50064 50189 50044 50074 50101 51719 50062 50065 50087 50167 50039 50084 51706 51707 50048 50161 50093 50206 50057 50081 50133 50040 50016 50120 50191 51701 50027 51700 50139 50004 50010 50024 50142 50079 50132 50050
- Product
- AXIOM Artis dFA, Model Number 7555373
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 39
- Distribution
- US Nationwide Distribution
- Recall date
- July 31, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)