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

Recall Z-0555-2024 — CARDIOHELP-i Heart Lung Support System- A blood oxygenation and carbon dioxide removal system used to pump blood through the extracorporeal bypass circuit for circulatory and/or pulmonary support for periods appropriate to cardiopulmonary bypass Part Number: 701072780, (CARDIOHELP-I US); 7010480

U.S. FDA — Device Enforcement · United States · 2023-11-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0555-2024
Date of alert
2023-11-06
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Maquet Medical Systems USA
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
04058863074863
Reported risk: Certain factory settings for the device were incorrectly described in the IFU-related to the warning limits for PVen and PAux, and the default settings for the venous bubble sensor (VBS) and the automatic lock in the Minimized Extracorporeal Circulation (MECC) ThApp
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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