DEFIGARD TOUCH 7 recall in Canada: Defibrillation shock may not be delivered
In plain language
This recall involves the DEFIGARD TOUCH 7 defibrillator sold in Canada. It's being recalled because it may fail to deliver a defibrillation shock or show an electrode fault when none is present. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check model/serial numbers if provided.
- Return, repair, or dispose of it as instructed.
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Affected products
DEFIGARD TOUCH 7
Model: 1-128-9900
Why this matters
Defibrillation shock may not be delivered
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: 1-128-9900
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?
Defibrillation shock may not be delivered
What should consumers do?
Stop using the product immediately. Check model/serial numbers if provided. Return, repair, or dispose of it as instructed.
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. Defibrillation shock may not be delivered
When was this product recalled?
This product was recalled on January 6, 2020.