ClearanceBrief
Recall Z-0600-2007 ยท DTQ Console, Heart-Lung Machine, Cardiopulmonary Bypass

Terumo Cardiovascular Systems Corp

Terumo Advanced Perfusion System 1, 4 inch diameter (small) Roller Pump; Model 801040.

DateJun 30, 2007 (initiated Sep 1, 2004)
StatusTerminated
ReasonThe internal ribbon cable may loosen from the roller pump display board, resulting in loss of local control and/or local display.
Root causeOther
ActionThe 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.
Quantity1,484 of both models
DistributionWorldwide: 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.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K022947ADVANCED PERFUSION SYSTEM 1 (100/120 VOLT),ADVANCED PERFUSION SYSTEM 1 (220/240 VOLT, ROLLER PUMPS (6, 4 INCH
Terumo Cardiovascular Systems Corp., Mar 20, 2003