Artis Pheno, Artis Icono Floor, Artis Icono Biplane, Artis Icono Ceiling With Software Version Ve50b

Recalling firm: Siemens Healthcare (NZ) Ltd
Product: ARTIS pheno, ARTIS icono floor, ARTIS icono biplane, ARTIS icono ceiling with software version VE50B. [Device]. Model: Catalogue/Lot number – ARTIS icono biplane - 11327600 with SW VE50B; ARTIS icono ceiling - 11328100 with SW VE50B; ARTIS icono floor - 11327700 with SW VE50B; ARTIS pheno - 10849000 with SW VE50B. Affected: With software VE50B
Reason: The manufacturer has identified that in certain operating situations, the system may fail to execute movement control commands as intended. If this occurs, motorised stand and/or table movement may no longer be available until the system has been completely restarted. The impact on system operation is that movement of the affected system axes may no longer be possible until the system is restarted., This may limit or delay the ability to change projection planes or to position the system as required for the intended procedure. In situations where immediate access to the patient or...
Classification: Class I
Category: medical device recall
Country: New Zealand
Agency: MEDSAFE
Recall date: 2026-09-29
Status: Ongoing
Distribution: New Zealand - Hospital/Pharmacy/Laboratory

Recall details on Nibble Recalls: https://trynibble.app/recalls/afc51206-c764-4d44-80b5-ffcc5f497909