ARTIS one with a hybrid cable- An angiography system developed for diagnostic imaging and interventional procedures. Material Number: 10848600
Reported: May 3, 2023 Initiated: March 21, 2023 #Z-1469-2023
Product Description
ARTIS one with a hybrid cable- An angiography system developed for diagnostic imaging and interventional procedures. Material Number: 10848600
Reason for Recall
Examination room monitor connected with the hybrid cable may have a display issue and no image function is available
Details
- Recalling Firm
- Siemens Medical Solutions USA, Inc
- Units Affected
- 4 units US
- Distribution
- 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.
- Location
- Malvern, PA
Frequently Asked Questions
What product was recalled? ▼
ARTIS one with a hybrid cable- An angiography system developed for diagnostic imaging and interventional procedures. Material Number: 10848600. Recalled by Siemens Medical Solutions USA, Inc. Units affected: 4 units US.
Why was this product recalled? ▼
Examination room monitor connected with the hybrid cable may have a display issue and no image function is available
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 3, 2023. Severity: Moderate. Recall number: Z-1469-2023.
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