XERF Effector 60 recall in Canada: potential for patient injury
In plain language
This recall involves the XERF Effector 60, a medical device sold in Canada. It's being recalled because a manufacturing issue could lead to tip failure and patient injury. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Customers will be contacted with instructions to return and replace affected units.
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Affected products
XERF Effector 60
Model: 1101210000, 1101210100, 1101210200
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Potential for patient injury
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: More than 10 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 1101210000, 1101210100, 1101210200
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?
Potential for patient injury
What should consumers do?
Stop using the product immediately. Customers will be contacted with instructions to return and replace affected units.
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. Potential for patient injury
When was this product recalled?
This product was recalled on September 16, 2025.
Is the Lutronic Corporation brand affected by this recall?
Yes, Lutronic Corporation products are affected by this recall. This recall involves the XERF Effector 60, a medical device sold in Canada. It's being recalled because a manufacturing issue could lead to tip failure and patient injury. Stop using the product and follow the return/repair steps in the official notice.