Grand Rapids, MI, United States
Surge Medical Sales, LLC (DBA Surge Cardiovascular) recalls
1 recall recorded since 2018, most recently on 18 July 2018. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 18 July 2018
- Terminated
- 4 April 2019
- Reason
- The device was built with the rigid insertion stylet instead of the flexible stylet.
- Distribution
- US Distribution to state of: SC.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0068-2019
- 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 introd
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.