Leksell GammaPlan® recall in Canada: Inconsistent alignment
In plain language
This recall involves Leksell GammaPlan® Version 11.4 software used in Canada. It's being recalled because a software issue could lead to inconsistent alignment and incorrect patient location for irradiation. Healthcare professionals should follow the instructions in the official notice.
What to do
- Elekta will notify affected customers directly.
- Follow the instructions in safety notice 100-01-102-019.
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Affected products
Leksell GammaPlan®
Model: VERSION 11.4
Lot: Not applicable.
Why this matters
Incorrect patient location for irradiation
Do I have this product?
This recall only applies to specific products. Follow the steps below to check.
- 1
Check the product name
Make sure your product name matches one of the affected products listed above.
- 2
Check the lot number
Lot numbers identify specific production batches.
Affected lots: Not applicable.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: VERSION 11.4
If your product matches one or more of the details above, it may be affected by this recall.
If your product does not match these details, it is not affected by this recall.
When in doubt, always check the official notice.
Frequently Asked Questions
Why was this product recalled?
Incorrect patient location for irradiation
What should consumers do?
Elekta will notify affected customers directly. Follow the instructions in safety notice 100-01-102-019.
Where was the product sold?
This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.
Is there a health risk?
Yes, there may be a health risk. Incorrect patient location for irradiation
When was this product recalled?
This product was recalled on December 23, 2025.
Is the Elekta Solutions Ab brand affected by this recall?
Yes, Elekta Solutions Ab products are affected by this recall. This recall involves Leksell GammaPlan® Version 11.4 software used in Canada. It's being recalled because a software issue could lead to inconsistent alignment and incorrect patient location for irradiation. Healthcare professionals should follow the instructions in the official notice.