device · product 1 of 1
iGUIDE Software 2.2 Product Usage: Control of accurate patient positioning with assistance of a 30 Tracking System in a radiotherapy environment.
- Recall number
- Z-3017-2017
- Initiated
- June 19, 2017
- Classification
- Class II
- Status
- Terminated
- Recalling firm
- Elekta, Inc.
- Quantity
- 110 units
App-derived interpretation
Incorrect PEC values.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Inspect official wording and provenance
Reason for recall
Incorrect PEC values.
Code information
Scope; iGUIDE 2.2.0, iGUIDE 2.2.1
Distribution pattern
Worldwide Distribution in the states of AK, CT, GA, KY, LA, MA, MD, MN, NC, NM, OH, OK, OR, PA, SC, SD, TN, TX, VA, WA and countries of Hawaii Australia, Austria, Belgium, Denmark, France, Germany, Hong Kong, India, Indonesia, Ireland, Italy, Japan, Netherlands, New Zealand, Poland, Slovenia, Spain, Sweden, Switzerland, United Kingdom, & Vietnam.