FDA recall Z-0841-2022

Siemens Medical Solutions USA, Inc · Class II · device

Product

Ysiosystem with VC10 software version, Model Number 10281013. Radiographic system

Reason for recall

Siemens Healthineers has identified a software error in previous software version VB10 for the Ysio fully automated system. The unit may process incorrect internal values for the position of its ceiling tube stand. If the user activates a longitudinal or transversal movement at the time of the error, the system controls may initiate a correction of the tube stand position, resulting in an unintended movement. If the described error occurs, a potential for collision risk for objects or persons in the vicinity of the moving stand exists. This may result in minor to serious injuries to persons.

Distribution

US Nationwide.

Key facts

Status
Ongoing
Initiation date
2022-01-31
Report date
2022-04-06
Voluntary/Mandated
Voluntary: Firm initiated
Location
Malvern, PA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0841-2022