PlainRecalls
FDA Devices Moderate Class II Terminated

Siemens AXIOM Artis zeego x-ray, angiographic system

Reported: August 21, 2013 Initiated: May 13, 2013 #Z-1945-2013

Product Description

Siemens AXIOM Artis zeego x-ray, angiographic system

Reason for Recall

Siemens issued a customer safety notice about the overlay of system information after a functional check of the brakes on the Artis Zeego system.

Details

Units Affected
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.
Location
Malvern, PA

Frequently Asked Questions

What product was recalled?
Siemens AXIOM Artis zeego x-ray, angiographic system. Recalled by Siemens Medical Solutions USA, Inc. Units affected: 132.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 21, 2013. Severity: Moderate. Recall number: Z-1945-2013.