Health product recall

Powerheart AED G5

Last updated

Summary

Product
Powerheart AED G5
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information. 

Affected 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

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Companies
Zoll Medical Corporation
269 Mill Road, Chelmsford, Massachusetts, United States, 01824
Published by
Health Canada
Audience
General public
Recall class
Type I
Identification number
RA-77474

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