Recall Monitor
Health Products

Infant/Child Reduced Energy Defibrillation Electrode

· Published by Health Canada · Official notice

Details

Alert type: Health product recall
Category: Health products - Medical devices - Cardiovascular
Product: Infant/Child Reduced Energy Defibrillation Electrode
Issue: Medical devices - Performance
What to do: Contact the manufacturer if you require additional information.
Audience: Healthcare, Industry
Recall class: Type II
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Products

Affected productsLot or serial numberModel or catalogue number
Infant/Child Reduced Energy Defibrillation Electrode31893111101-000016
Infant/Child Reduced Energy Defibrillation Electrode31563911101-000016
Infant/Child Reduced Energy Defibrillation Electrode31530311101-000016
Infant/Child Reduced Energy Defibrillation Electrode31600711101-000016
Infant/Child Reduced Energy Defibrillation Electrode32052911101-000016
Infant/Child Reduced Energy Defibrillation Electrode31585811101-000016
Infant/Child Reduced Energy Defibrillation Electrode31893111101-000017
Infant/Child Reduced Energy Defibrillation Electrode31563911101-000017
Infant/Child Reduced Energy Defibrillation Electrode31530311101-000017
Infant/Child Reduced Energy Defibrillation Electrode31600711101-000017
Infant/Child Reduced Energy Defibrillation Electrode32052911101-000017
Infant/Child Reduced Energy Defibrillation Electrode31585811101-000017

Issue

On November 21, 2024 Stryker began investigating product complaints related to the gel delamination of pediatric electrodes.

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