Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1938-2019 — Powerheart¿ G5 Automatic AED

U.S. FDA — Device Enforcement · United States · 2019-06-04 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1938-2019
Date of alert
2019-06-04
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Cardiac Science Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00812394021222
Reported risk: Sub-supplier s documentation for specific Printed Circuit Boards (PCB) is insufficient to determine if the devices conform to specifications.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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