Terumo Cardiovascular Systems Corporation Terumo Advanced Perfusion System 1 base, 110/120V; 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, 110/120V; 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, 110/120V; Model 801763. For use for up to 6 hours in the e due to Local pump controls including start/stop button, select button and manual button may not function.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Local pump controls including start/stop button, select button and manual button may not function.
Recommended Action
Per FDA guidance
Consignees were notified by recall letter dated 7/18/08 and were provided with revised operating instructions telling them to revert to the central control module should these problems occur.
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