Health product recall

Infant/Child Reduced Energy Defibrillation Electrode

Last updated

Summary

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

Affected products

Affected products Lot or serial number Model or catalogue number
Infant/Child Reduced Energy Defibrillation Electrode 318931 11101-000016
Infant/Child Reduced Energy Defibrillation Electrode 315639 11101-000016
Infant/Child Reduced Energy Defibrillation Electrode 315303 11101-000016
Infant/Child Reduced Energy Defibrillation Electrode 316007 11101-000016
Infant/Child Reduced Energy Defibrillation Electrode 320529 11101-000016
Infant/Child Reduced Energy Defibrillation Electrode 315858 11101-000016
Infant/Child Reduced Energy Defibrillation Electrode 318931 11101-000017
Infant/Child Reduced Energy Defibrillation Electrode 315639 11101-000017
Infant/Child Reduced Energy Defibrillation Electrode 315303 11101-000017
Infant/Child Reduced Energy Defibrillation Electrode 316007 11101-000017
Infant/Child Reduced Energy Defibrillation Electrode 320529 11101-000017
Infant/Child Reduced Energy Defibrillation Electrode 315858 11101-000017

Issue

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

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Companies

Physio-Control, Inc.

11811 Willows Road North East, Redmond, Washington, United States, 98052

Published by
Health Canada
Audience
Healthcare
Industry
Recall class
Type II
Recall date
Identification number
RA-81539

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