Elekta Unity recall in Canada: Legionella risk
In plain language
This recall involves the Elekta Unity medical device sold in Canada. It's being recalled because there is a potential risk of Legionella bacteria in the heat exchanger condensation collection tray. This risk is only for service users working directly on the tray.
What to do
- Stop using the product immediately.
- Check model/serial numbers if provided.
- Follow the return/repair steps in the official notice.
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Affected products
Elekta Unity
Model: 1536549
Why this matters
Legionella risk
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 model number
Model numbers are typically on the product label or packaging.
Affected models: 1536549
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?
Legionella risk
What should consumers do?
Stop using the product immediately. Check model/serial numbers if provided. Follow the return/repair steps in the official notice.
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. Legionella risk
When was this product recalled?
This product was recalled on June 5, 2020.
Is the Elekta brand affected by this recall?
Yes, Elekta products are affected by this recall. This recall involves the Elekta Unity medical device sold in Canada. It's being recalled because there is a potential risk of Legionella bacteria in the heat exchanger condensation collection tray. This risk is only for service users working directly on the tray.