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Siemens Medical Solutions USA, Inc recalls ARTIS one with a hybrid cable- An angiography system developed for diagnostic imaging and interventional procedures. Ma
Recalled May 3, 2023 · FDA recall Z-1469-2023 · Siemens Medical Solutions USA
Hazard
Examination room monitor connected with the hybrid cable may have a display issue and no image function is available · FDA Class II
Units
4 units US
Sold at
Worldwide - US Nationwide distribution in the states of FL, SD, PR and the countries of Angola, Argentina, Australia, Brazil, Bulgaria, China, Georgia, Germany, India, Indonesia, Iraq, Japan, Malaysia, Morocco, Nepal, Nigeria, Poland, Russia, Rwanda, Serbia, Slovenia, South Africa, Spain, Sudan, Syria, Taiwan, Thailand, Uganda, Ukraine, United Kingdom, Uzbekistan, Vietnam.
Description
Examination room monitor connected with the hybrid cable may have a display issue and no image function is available
Product
ARTIS one with a hybrid cable- An angiography system developed for diagnostic imaging and interventional procedures. Material Number: 10848600
Manufacturer(s)
Siemens Medical Solutions USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →