FRED easyport recall in Canada: Defibrillator may malfunction
In plain language
This recall involves the FRED easyport defibrillator sold in Canada. It's being recalled because a defect in the electrode cable can cause the device to malfunction. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Return or repair it as instructed.
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Affected products
FRED easyport
Model: 0.900000
Why this matters
Defibrillator malfunction
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: 0.900000
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?
Defibrillator malfunction
What should consumers do?
Stop using the product immediately. Return or repair 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. Defibrillator malfunction
When was this product recalled?
This product was recalled on May 14, 2019.
Is the FRED brand affected by this recall?
Yes, FRED products are affected by this recall. This recall involves the FRED easyport defibrillator sold in Canada. It's being recalled because a defect in the electrode cable can cause the device to malfunction. Stop using the product and follow the return/repair steps in the official notice.