Cardiac Science Corporation: Medical Device Recall in 2019 - (Recall #: Z-1938-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Powerheart¿ G5 Automatic AED

Product Classification:

Class II

Date Initiated: June 4, 2019

Date Posted: July 10, 2019

Recall Number: Z-1938-2019

Event ID: 83103

Reason for Recall:

Sub-supplier s documentation for specific Printed Circuit Boards (PCB) is insufficient to determine if the devices conform to specifications.

Status: Terminated

Product Quantity: 5 devices

Code Information:

Model Number G5A 80A; AED Serial Number (UDI Number): D00000133922 )(01)00812394021222(11)190508(21)D00000133922), D00000133927 ((01)00812394021222(11)190509(21)D00000133927), D00000133930 ((01)00812394021222(11)190509(21)D00000133930), D00000133934 ((01)00812394021222(11)190509(21)D00000133934), D00000133936 )(01)00812394021222(11)190509(21)D00000133936).

Distribution Pattern:

US distribution to Georgia, Texas, and Wisconsin.

Voluntary or Mandated:

Voluntary: Firm initiated