Public recall detail

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

2024-06-17

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Recall Safety notice
Quick summary

Quick summary: Powerheart AED G5 Semi-Automatic and Powerheart AED G5 Semi-Automatic With CPR Assist. Date: 2024-06-17.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Powerheart AED G5 Semi-Automatic and Powerheart AED G5 Semi-Automatic With CPR Assist. Date: 2024-06-17.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandZoll Medical Corporation
ProductPowerheart AED G5 Semi-Automatic and Powerheart AED G5 Semi-Automatic With CPR Assist
IssueMedical devices - Performance
Recall classType I
IdentificationRA-75683

Affected products

ProductPowerheart Aed G5 Semi-Automatic With Cpr Assist
LotMore than 10 numbers, contact manufacturer.
ModelG5S-91C G5S-90C
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionPowerheart Aed G5 Semi-Automatic With Cpr Assist
ProductPowerheart Aed G5 Semi-Automatic
LotMore than 10 numbers, contact manufacturer.
ModelG5S-90A G5S-91A
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionPowerheart Aed G5 Semi-Automatic

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

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Cardiovascular
CompaniesZoll Medical Corporation 269 Mill Road, Chelmsford, Massachusetts, United States, 01824
Published byHealth Canada
Recall classType I
Alert / recall typeHealth product recall
Identification numberRA-75683
Background{}
CompaniesZoll Medical Corporation 269 Mill Road, Chelmsford, Massachusetts, United States, 01824
AudiencesHealthcare
Source updated2024-06-17

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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