Z-0601-2007

Terumo Advanced Perfusion System 1, 6 inch diameter (Large) Roller Pump; Model 801041

Name: Z-0601-2007 Terumo Advanced Perfusion System 1, 6 inch diameter (Large) Roller Pump; Model 801041
Creator: Terumo Cardiovascular Systems Corp
Published: 2004-09-01
License: https://open.fda.gov/license/

Terumo Cardiovascular Systems Corporation / initiated 2004-09-01 / Terminated

FDA source

Terumo Cardiovascular Systems Corp began a recall of Terumo Advanced Perfusion System 1, 6 inch diameter (Large) Roller Pump; Model 801041 on 2004-09-01. The reason FDA records is "The internal ribbon cable may loosen from the roller pump display board, resulting in loss of local control and/or local display". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0601-2007
Status: Terminated
Initiated: 2004-09-01
Posted: 2007-06-30
Terminated: 2009-07-07
Recalling firm: Terumo Cardiovascular Systems Corporation
Product: Terumo Advanced Perfusion System 1, 6 inch diameter (Large) Roller Pump; Model 801041.
Product code: DTQ Console, Heart-Lung Machine, Cardiopulmonary Bypass
Reason for recall: The internal ribbon cable may loosen from the roller pump display board, resulting in loss of local control and/or local display.
FDA root cause: Other
Action: 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.
Quantity in commerce: 1,484 of both models
Distribution: Worldwide: USA, Australia, Belgium, Canada, Dominican Republic, Egypt, Germany, Hong Kong, India, Indonesia, Japan, Korea, Mexico, Malaysia, Singapore, South Africa, Taiwan, Thailand and United Arab Emirates.
Product codes and lots: Serial numbers 0030 through 0998 may be affected. Serial numbers 0052, 0418, 0559, 0745 and 0767 have been corrected.

Product code DTQ

K022947Class IIAdvanced Perfusion System 1 (100/120 Volt),advanced Perfusion System 1 (220/240 Volt, Roller Pumps (6, 4 InchTerumo Cardiovascular Systems Corp. / cleared 2003-03-20

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)