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Surge Medical Sales, LLC (DBA Surge Cardiovascular) recalls Retrograde Cardioplegia Cannula, Model Number RMG-0015S The Retrograde Cardioplegia Cannula is intended for use in p
Recalled October 10, 2018 · FDA recall Z-0068-2019 · Surge Medical Sales, LLC (DBA Surge Cardiovascular)
Hazard
The device was built with the rigid insertion stylet instead of the flexible stylet. · FDA Class II
Units
35 units
Sold at
US Distribution to state of: SC.
Description
The device was built with the rigid insertion stylet instead of the flexible stylet.
Product
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.
Manufacturer(s)
Surge Medical Sales, LLC (DBA Surge Cardiovascular)
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →