Terumo Cardiovascular Systems Corporation Terumo Advanced Perfusion System 1 Base, 100/120V; Model 801763. For use for up to 6 hours in the extracorporeal circulation of blood for arterial perfusion, regional perfusion and cardiopulmonary bypass procedures. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Terumo Advanced Perfusion System 1 Base, 100/120V; Model 801763. For use for up to 6 hours in the extracorporeal circulation of blood for arterial perfusion, regional perfusion and cardiopulmonary bypass procedures.
Brand
Terumo Cardiovascular Systems Corporation
Lot Codes / Batch Numbers
Serial numbers 0013 through 0610 and 1001 through 1026.
Products Sold
Serial numbers 0013 through 0610 and 1001 through 1026.
Terumo Cardiovascular Systems Corporation is recalling Terumo Advanced Perfusion System 1 Base, 100/120V; Model 801763. For use for up to 6 hours in the e due to The pumps may exhibit blank or distorted displays, loss of local control and/or may have local control knobs that are difficult to use.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The pumps may exhibit blank or distorted displays, loss of local control and/or may have local control knobs that are difficult to use.
Recommended Action
Per FDA guidance
Consignees were notified via letter dated 7/18/08 and instructed to use the central control module should the problem occur. Contact Terumo Cardiovascular Systems Corp at 1-800-521-2818 for assistance.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026