ARTIS pheno, ARTIS icono biplane, and ARTIS icono floor
Reported: January 25, 2023 Initiated: December 16, 2022 #Z-0956-2023
Product Description
ARTIS pheno, ARTIS icono biplane, and ARTIS icono floor
Reason for Recall
Mechanical connection between the tabletop and table base may be lost.
Details
- Recalling Firm
- Siemens Medical Solutions USA, Inc
- Units Affected
- 550 units
- Distribution
- Worldwide distribution - US Nationwide and the countries of Armenia, Australia, Austria, Belgium, Bulgaria, Canada, Chile, China, Colombia, Czech Republic, Denmark, Egypt, Finland, France, Germany, Greece, Hong Kong, India, Indonesia, Iran, Ireland, Italy, Japan, Kazakhstan, Kuwait, Lebanon, Monaco, Netherlands, New Zealand, Norway, Oman, Poland, Qatar, Russian Federation, Saudi Arabia, Singapore, Slovakia, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, United Arab Emirates, United Kingdom, and Vietnam.
- Location
- Malvern, PA
Frequently Asked Questions
What product was recalled? ▼
ARTIS pheno, ARTIS icono biplane, and ARTIS icono floor. Recalled by Siemens Medical Solutions USA, Inc. Units affected: 550 units.
Why was this product recalled? ▼
Mechanical connection between the tabletop and table base may be lost.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 25, 2023. Severity: Moderate. Recall number: Z-0956-2023.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11