device · product 1 of 1
iGUIDE System Product Usage: The intended use of the device is the control of accurate patient positioning with the assistance of a 30 Tracking System in a radiotherapy environment.
- Recall number
- Z-1807-2014
- Initiated
- May 29, 2014
- Classification
- Class II
- Status
- Terminated
- Recalling firm
- Elekta, Inc.
- Quantity
- 224
App-derived interpretation
bug in the software prevents the iGUIDE software
Official device-enrichment evidence · Sourced
Software design
Inspect official wording and provenance
Reason for recall
A bug in the software prevents the iGUIDE software from logging off.
Code information
Software Versions 2.0.0, 2.0.1 and 2.0.2
Distribution pattern
Worldwide Distribution - USA (nationwide) in the states of AZ, CA, CT, HI, IL, IA, KY, MD, MA, MI, MO, NH, NJ, NC, ND, OH, OK, OR, PA, TX, VA, WA, WI, and the countries of Algeria, Australia, Austria, Brazil, Canada, China, Colombia, Denmark, Finland, France, Germany, Hong Kong, India, Italy, Japan, Kazakhstan, Mexico, Netherlands, New Zealand, Peru, Poland, Russia, Saudi Arabia, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, United Kingdom and Vietnam