FDANovember 19, 2019device

TandemLife ECLS Procedure Kit - V24/A17, Catalog Number 5740-2417 - Product Usage: The function of the 24Fr ProtekSolo Venous Cannula is to provide a conduit for blood to travel from the patient s venous system when connected to accessory extracorporeal equipment. The Venous Cannula is intended t...

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

The hazard

The kit contained a 29Fr ProtekDuo cannula instead of a 24Fr Protek Solo Venous cannula.

What to do

FDA enforcement status: Terminated

Brands named

cardiac assistcardiac

UPCs

00814112020517

Recall history

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

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