Terumo Cardiovascular Systems Corp Terumo Advanced Perfusion System 1, 6 inch diameter Roller Pump; Model 801041. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Terumo Advanced Perfusion System 1, 6 inch diameter Roller Pump; Model 801041.
Brand
Terumo Cardiovascular Systems Corp
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Serial number range 0033 through 1308 may be affected by this problem. Serial numbers 1060 and 1148 have been corrected.
Terumo Cardiovascular Systems Corp is recalling Terumo Advanced Perfusion System 1, 6 inch diameter Roller Pump; Model 801041. due to The tube clamp mechanism on the roller pump may not open when the rotation knob is turned, making it difficult to remove and/or insert tubing.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The tube clamp mechanism on the roller pump may not open when the rotation knob is turned, making it difficult to remove and/or insert tubing.
Recommended Action
Per FDA guidance
The firm is visiting the consignees as complaints are received and making corrections. Corrections were made in August 2005 and April 2006 to date. Other units will be repaired if complaints are received and the firm issued a Device Correction Letter dated 6/6/07 notifying all users of the problem and appropriate action to take 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 noticeDistribution
As reported by FDA
GA
Page updated: Jan 10, 2026