FDAJuly 18, 2018device

Retrograde Cardioplegia Cannula, Model Number RMG-0015S The Retrograde Cardioplegia Cannula is intended for use in perfusing cardioplegia solutions retrograde through the coronary sinus by means of transatrial introduction.

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

The hazard

The device was built with the rigid insertion stylet instead of the flexible stylet.

What to do

FDA enforcement status: Terminated

Brands named

surge medical sales llc dba surge cardiovascularsurgesurge medical

UPCs

00794030718

Recall history

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

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