Terumo Cardiovascular Systems Corp Terumo Advanced Perfusion System 1, 4 inch diameter Roller Pump; Model 801040. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Terumo Advanced Perfusion System 1, 4 inch diameter Roller Pump; Model 801040.
Brand
Terumo Cardiovascular Systems Corp
Lot Codes / Batch Numbers
Serial numbers 0031 through 0324 are potentially affected by the problem. Serial numbers 0092, 0128, 0152, 0223, 0226, 0237, 0246, 0260 and 0296 have been corrected.
Products Sold
Serial numbers 0031 through 0324 are potentially affected by the problem. Serial numbers 0092, 0128, 0152, 0223, 0226, 0237, 0246, 0260 and 0296 have been corrected.
Terumo Cardiovascular Systems Corp is recalling Terumo Advanced Perfusion System 1, 4 inch diameter Roller Pump; Model 801040. due to A belt slip message may be displayed on the roller pump due to low belt tension or the presence of grease.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
A belt slip message may be displayed on the roller pump due to low belt tension or the presence of grease.
Recommended Action
Per FDA guidance
The firm is visiting consignees and making corrections as complaints are received. These corrections, to date, have been made between 04/04 and 09/06. The firm will correct other units as complaints are received and issued a Device Correction Letter dated 6/6 /07 notifying all users of the problem and appropriate responses should it 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