iGUIDE System, for patient positioning, with assistance of a 30 Tracking System in a radiotherapy environment.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Software iGUIDE 2.1 and 2.2
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Elekta, Inc.
- Reason for Recall:
- If by mistake the initial pre-treatment imaging was performed BEFORE the HexaPOD was moved to the DRIVE (*START) position, iGUIDE offers the possibility to branch into a specific catch-up workflow, which was implemented to use the initial scan data.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
iGUIDE System, for patient positioning, with assistance of a 30 Tracking System in a radiotherapy environment.
Product Codes/Lot Numbers:
Software iGUIDE 2.1 and 2.2
Distribution:
Distributed in: IL, LA
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1705-2016
Related Recalls
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Elekta has identified that if the microswitch within the middle arm is incorrectly setup, there is a potential for an uncontrolled extension of iViewGT / XVI detector arms. When the detector arm is fully deployed there is no risk of uncontrolled extension.