Siemens AXIOM Artis zeego x-ray recall
Siemens AXIOM Artis zeego x-ray, angiographic system
Why was Siemens AXIOM Artis zeego x-ray recalled?
Siemens issued a customer safety notice about the overlay of system information after a functional check of the brakes on the Artis Zeego system.
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 number 10280959
- Product
- Siemens AXIOM Artis zeego x-ray, angiographic system
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 132
- Distribution
- Nationwide distribution: AL, AK, AR, AZ, CA, CO, CT, DC, FL, GA, IA, IL, IN, KY, LA, MA, MD, MN, MO,MS, NC, NE, NH, NJ, NY, OH, PA, PR, SD, TN, TX, UT, VA, WA, and WI.
- Recall date
- August 21, 2013
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)