Terumo Cardiovascular Systems Corp Terumo Advanced Perfusion System, 1 Roller Pump, 4 inch diameter; Catalog No. 801040, Terumo Cardiovascular Systems, Ann Arbor, MI 48103 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Terumo Advanced Perfusion System, 1 Roller Pump, 4 inch diameter; Catalog No. 801040, Terumo Cardiovascular Systems, Ann Arbor, MI 48103
Brand
Terumo Cardiovascular Systems Corp
Lot Codes / Batch Numbers
Serial Numbers 2110 through 2125.
Products Sold
Serial Numbers 2110 through 2125.
Terumo Cardiovascular Systems Corp is recalling Terumo Advanced Perfusion System, 1 Roller Pump, 4 inch diameter; Catalog No. 801040, Terumo Cardiov due to Failure to operate; The pump may fail to operate, and be difficult to hand crank, due to an internal electrical short condition.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Failure to operate; The pump may fail to operate, and be difficult to hand crank, due to an internal electrical short condition.
Recommended Action
Per FDA guidance
Consignees were notified via an Urgent Medical Device Correction letter dated 9/10/07, which provided them guidance in the event the problem occurs and advised them they would be contacted to schedule replacement of the circuit boards.
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 noticeDistribution
As reported by FDA
AL, AZ, FL, IL, IN, MS, NE, NC, PA, VA
Page updated: Jan 10, 2026