The Sarns Centrifugal Pump is a single use device sterilized by ethylene oxide gas. The device is sold single sterile in cartons of 8 units, or may be provided in bulk, non-sterile to another Terumo location for inclusion in Cardiovascular Procedure Kits. Cardiovascular Procedure kits are packaged individually.
This recall has been terminated (originally issued February 22, 2017).
- Recall Initiated
- May 27, 2015
- Posted
- February 22, 2017
- Terminated
- February 23, 2017
- Recall Number
- Z-1235-2017
- Quantity
- 579 units have entered into the distribution chain
- Firm Location
- Elkton, MD
- Official Source
- View on FDA website ↗
Reason for Recall
Terumo Cardiovascular Systems Corporation has received complaints indicating that the Sarns Centrifugal Pump (disposable pump heads) have exhibited leaks. The leaks were detected during priming of the bypass circuit and during CPB procedures. In each of the reported incidents, there were no reports of patient injury as a result of the centrifugal pump leaks. Terumo Cardiovascular System's investigation into the incident has identified the cause of the leaks to be cracks in both the Top Housing and Magnet Back Housing of the pump. When the cracks cause the housing to become compromised, it is possible for fluid to leak from the pump head.
Distribution
Terumo CVS has identified 33 domestic consignees and 0 international consignee that are affected by this recall
Lot / Code Info
TAOS, TC03
Root Cause
Process control
Action Taken
Customer Notification Letter/Response Form is being sent to all affected consignees.