Consumer product recall in Canada: ZOLL AED Pro may fail during use
In plain language
This recall involves the ZOLL AED Pro External Defibrillator sold in Canada. It's being recalled because it may fail to deliver a shock during a defibrillation attempt. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check model numbers if provided.
- Return, repair, or dispose of it as instructed.
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Affected products
ZOLL AED Pro External Defibrillator
Model: ZOLL AED PRO
Why this matters
Failure to deliver therapy
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: ZOLL AED PRO
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?
Failure to deliver therapy
What should consumers do?
Stop using the product immediately. Check model 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. Failure to deliver therapy
When was this product recalled?
This product was recalled on June 18, 2019.
Is the ZOLL brand affected by this recall?
Yes, ZOLL products are affected by this recall. This recall involves the ZOLL AED Pro External Defibrillator sold in Canada. It's being recalled because it may fail to deliver a shock during a defibrillation attempt. Stop using the product and follow the return/repair steps in the official notice.