Every recall we track for C-RAD POSITIONING AB — 3 in all — plus the complaints and injury reports the public filed about them.
C-RAD Catalyst positioning devices with specific models may misposition patients during stereotactic radiosurgery, risking treatment failure. Affected units include SP001-0026 and SP003-0002 models. Contact C-RAD for details.
C-RAD Catalyst+ C4D software (version 6.5.1 SP2) used with Catalyst devices may cause incorrect patient rotation in scans. Affected models include Catalyst, Catalyst HD, Catalyst PT, Catalyst X4, and Catalyst+ series. Recalls due to software scanning error.
C-RAD Positioning software versions 6.1.1 and 6.1.0 have a setup sync problem that may cause incorrect site changes. Affected users should contact C-RAD for details.
