Surge Medical Sales, LLC (DBA Surge Cardiovascular): Medical Device Recall in 2018 - (Recall #: Z-0068-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: July 18, 2018

Date Posted: October 10, 2018

Recall Number: Z-0068-2019

Event ID: 81042

Reason for Recall:

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

Status: Terminated

Product Quantity: 35 units

Code Information:

Lot code: 00794-030718

Distribution Pattern:

US Distribution to state of: SC.

Voluntary or Mandated:

Voluntary: Firm initiated