Digital TENS/EMS recall in Canada: Unauthorized device
In plain language
This recall involves Digital TENS/EMS devices sold in Canada. It's being recalled because the device was sold after its licence expired, making it an unauthorized medical device. Stop using the product and contact OrthoCanada if you purchased it from them between April 1, 2022, and December 2, 2022.
What to do
- Stop using the product immediately.
- Contact OrthoCanada if you purchased the product from them between April 1, 2022, and December 2, 2022.
Get alerts for recalls like this
Get email alerts when new recalls affect products in this category.
Affected products
Digital TENS/EMS
Model: EV-906
Lot: More than 10 numbers, contact manufacturer.
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: EV-906
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?
This recall involves Digital TENS/EMS devices sold in Canada. It's being recalled because the device was sold after its licence expired, making it an unauthorized medical device. Stop using the product and contact OrthoCanada if you purchased it from them between April 1, 2022, and December 2, 2022.
What should consumers do?
Stop using the product immediately. Contact OrthoCanada if you purchased the product from them between April 1, 2022, and December 2, 2022.
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?
A potential safety risk has been identified with this product. Stop using it immediately and follow the instructions in the official recall notice.
When was this product recalled?
This product was recalled on January 13, 2023.
Is the Everyway Medical Instruments Co Ltd brand affected by this recall?
Yes, Everyway Medical Instruments Co Ltd products are affected by this recall. This recall involves Digital TENS/EMS devices sold in Canada. It's being recalled because the device was sold after its licence expired, making it an unauthorized medical device. Stop using the product and contact OrthoCanada if you purchased it from them between April 1, 2022, and December 2, 2022.