Health product recall

Powerheart AED G5 Semi-Automatic and Powerheart AED G5 Semi-Automatic With CPR Assist

Last updated

Summary

Product
Powerheart AED G5 Semi-Automatic and Powerheart AED G5 Semi-Automatic With CPR Assist
Issue
Medical devices - Performance issue
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalogue number

Powerheart Aed G5 Semi-Automatic With Cpr Assist

More than 10 numbers, contact manufacturer.

G5S-91C
G5S-90C

Powerheart Aed G5 Semi-Automatic

More than 10 numbers, contact manufacturer.

G5S-90A
G5S-91A

Issue

The G5 Semi-Automatic AED is shipped, with a protective film over its front panel, to protect the screen and shock button from cosmetic damage during shipping. It has come to manufacturer’s   attention that customers may not be removing the protective film during deployment of the product. If the protective film is left adhered to the front bezel it may prevent the user from actuating the shock button. This may lead to a delay or prevent delivery of defibrillation therapy to a victim suffering from sudden cardiac arrest.

Recall start date: June 10, 2024

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
Healthcare
Recall class
Type I
Identification number
RA-75683

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