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Cardiac Science Corporation recalls Powerheart¿ G5 Automatic AED
Recalled July 10, 2019 · FDA recall Z-1938-2019 · Cardiac Science
Hazard
Sub-supplier s documentation for specific Printed Circuit Boards (PCB) is insufficient to determine if the devices conform to specifications. · FDA Class II
Units
5 devices
Sold at
US distribution to Georgia, Texas, and Wisconsin.
Description
Sub-supplier s documentation for specific Printed Circuit Boards (PCB) is insufficient to determine if the devices conform to specifications.
Product
Powerheart¿ G5 Automatic AED
Manufacturer(s)
Cardiac Science Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →