Powerheart AED G5 recall in Canada: performance issue
In plain language
This recall involves Powerheart AED G5 devices sold in Canada. They are being recalled because they may fail self-tests due to prolonged exposure to extreme temperatures or humidity. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check the model numbers provided.
- Contact the manufacturer for additional information.
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Affected products
Powerheart AED G5 Semi-Automatic
Model: G5S-90A, G5S-91A
Lot: More than 10 numbers, contact manufacturer.
Powerheart AED G5 Semi-Automatic With Cpr Assist
Model: G5S-90C, G5S-91C
Lot: More than 10 numbers, contact manufacturer.
Powerheart AED G5 Automatic
Model: G5A-90A, G5A-90C, G5A-91A, G5A-91C
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Performance issue
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: G5A-90A, G5A-90C, G5A-91A, G5A-91C, G5S-90A, G5S-90C, G5S-91A, G5S-91C
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?
Performance issue
What should consumers do?
Stop using the product immediately. Check the model numbers provided. Contact the manufacturer for additional information.
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. Performance issue
When was this product recalled?
This product was recalled on May 21, 2025.
Is the Zoll Medical Corporation brand affected by this recall?
Yes, Zoll Medical Corporation products are affected by this recall. This recall involves Powerheart AED G5 devices sold in Canada. They are being recalled because they may fail self-tests due to prolonged exposure to extreme temperatures or humidity. Stop using the product and follow the return/repair steps in the official notice.