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All product recalls associated with Cardiac Science Corporation.
Total Recalls
26
Past Year
0
Class I (Serious)
0
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.
Sub-supplier s documentation for specific Printed Circuit Boards (PCB) is insufficient to determine if the devices conform to specifications.
The K302 relay switch of the G3 series AED product line may experience an early failure. If the K302 contacts are open at the time of rescue, there is a possible delay in therapy or failure to deliver therapy.
Potential for devices not to deliver therapy