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Cardiac Science Corporation

Cardiac Science Corporation Recalls

All product recalls associated with Cardiac Science Corporation.

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Recall Summary

Total Recalls

Past Year

Class I (Serious)

Most Recent

Jun 2019

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 21–26 of 26 recalls

Cardiac Science Corporation: Cardio Vive 92532 AED, BURDICK Manufactured by Cardiac S...

Potential for AED to not deliver defibrillation therapy.

FDAOct 13, 2008PR• Cardiac Science Corporation

Cardiac Science Corporation: Cardiac Science Powerheart Automated External Defibrillat...

Potential for AED to not deliver defibrillation therapy.

FDAOct 13, 2008PR• Cardiac Science Corporation

Cardiac Science Corporation: GE Responder 2019198 AED Manufactured for GE Medical Sys...

Potential for AED to not deliver defibrillation therapy.

FDAOct 13, 2008PR• Cardiac Science Corporation

Page 2 of 2Next

Cardiac Science Corporation: 9051 Electrode Adapter; Automated external defibrillator,...

Adaptor Cable Incorrectly Manufactured: The red and white connector ends of the adapter are switched. Therefore, the cable will not connect to the electrodes as indicated in the instructions.

FDAJan 23, 2008Nationwide• Cardiac Science Corporation

Cardiac Science Corporation: Electrode Adaptor Cable Quick-Combo System, Model 9055 Th...

Instructions For Use is not clear about how the AED voice and text prompts will differ when the adapter is used.

FDAJan 23, 2008Nationwide• Cardiac Science Corporation

Cardiac Science Corporation: Powerheart AED G3 Automated External Defibrillator Model ...

Some Powerheart AED Model 9300A may contain a suspect electronic component and there is a remote likelihood that the function of this device may be interrupted during the charge.

FDAJan 27, 2006Nationwide• Cardiac Science Corporation