Surge Medical Sales Retrograde Cardioplegia Cannula, Model Number RMG-0015S The Retrograde recall — FDA Z-0068-2019
The device was built with the rigid insertion stylet instead of the flexible stylet.
Overview of recall records associated with Surge Medical Sales, LLC (DBA Surge Cardiovascular), including dates, categories and classifications where available.
Classification mix: Class II: 1.
The device was built with the rigid insertion stylet instead of the flexible stylet.
This page summarizes recall records in which the official source identifies Surge Medical Sales, LLC (DBA Surge Cardiovascular) as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.