Terumo Cardiovascular Systems Corp Terumo Advanced Perfusion System 1, 4 inch diameter (small) 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 (small) Roller Pump; Model 801040.
Brand
Terumo Cardiovascular Systems Corp
Lot Codes / Batch Numbers
Serial numbers 0020 through 0899 may be affected. Serial numbers 0170, 0226 and 0739 have been corrected.
Products Sold
Serial numbers 0020 through 0899 may be affected. Serial numbers 0170, 0226 and 0739 have been corrected.
Terumo Cardiovascular Systems Corp is recalling Terumo Advanced Perfusion System 1, 4 inch diameter (small) Roller Pump; Model 801040. due to The internal ribbon cable may loosen from the roller pump display board, resulting in loss of local control and/or local display.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The internal ribbon cable may loosen from the roller pump display board, resulting in loss of local control and/or local display.
Recommended Action
Per FDA guidance
The firm corrected units in the field or brought them back for evaluation and repair as complaints were received between 9/04 and 4/06. The firm issued a Device Correction Letter dated 6/6/07 notifying all users of the problem and advising them that they will be visited and their units upgraded as replacement components become available.
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