Recall MonitorHealth ProductsType I recall
Powerheart AED G5
· Published by Health Canada · Official notice
Details
Alert type: Health product recall
Category: Health products - Medical devices - Cardiovascular
Product: Powerheart AED G5
Issue: Medical devices - Performance
What to do: Contact the manufacturer if you require additional information.
Audience: General public
Recall class: Type I
Products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| Powerheart AED G5 Semi-Automatic | More than 10 numbers, contact manufacturer. | G5S-90A G5S-91A |
| Powerheart AED G5 Semi-Automatic With Cpr Assist | More than 10 numbers, contact manufacturer. | G5S-91C G5S-90C |
| Powerheart AED G5 Automatic | More than 10 numbers, contact manufacturer. | G5A-91C G5A-90C G5A-91A G5A-90A |
Issue
Notify users of the potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity). Ensure that users monitor the device's self-test status to mitigate clinical failures. Recall start date: February 27, 2025