FDAApril 15, 2024device

CARDIOHELP-i System. Blood oxygenation and carbon dioxide removal system.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The firm identified that the measured patient leakage current in some devices significantly exceeded expected levels.

What to do

FDA enforcement status: Ongoing

Brands named

maquet medical systemsmaquetmaquet medical

UPCs

04037691658384

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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CARDIOHELP-i System. Blood oxygenation and carbon dioxide removal system. — Recall Details · AllClear