Terumo Cardiovascular Systems Corp Terumo Advanced Perfusion System 1 Roller Pump 6 inch diameter; Catalog No. 801041. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Terumo Advanced Perfusion System 1 Roller Pump 6 inch diameter; Catalog No. 801041.
Brand
Terumo Cardiovascular Systems Corp
Lot Codes / Batch Numbers
Serial numbers 0033 through 1263.
Products Sold
Serial numbers 0033 through 1263.
Terumo Cardiovascular Systems Corp is recalling Terumo Advanced Perfusion System 1 Roller Pump 6 inch diameter; Catalog No. 801041. due to The roller pump speed control knobs and the centrifugal pump speed control knobs may fail to function/change pump speed.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The roller pump speed control knobs and the centrifugal pump speed control knobs may fail to function/change pump speed.
Recommended Action
Per FDA guidance
The firm replaced the graphics driver board on complaint units as user complaints were received. The firm notified all users of the problem and the presence of an alternative method of pump speed control via recall letter dated 6/30/06.
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