ClearanceBrief
Recall Z-1002-2007 ยท DTQ Console, Heart-Lung Machine, Cardiopulmonary Bypass

Terumo Cardiovascular Systems Corp

Terumo Perfusion System 8000 Roller Pump, 115V; Model 8000; Catalog No. 16402.

DateJul 7, 2007 (initiated Jul 1, 2004)
StatusTerminated
ReasonRoller Pump: Due to a circuit board malfunction the roller pumps may stop during use without displaying an error message, may stop during use with an overspeed error posted on the local display, or may fail to start/restart resulting in the pump(s) being non-functional.
Root causeOther
ActionAs the complaints were received (between 07/04 and 01/06), the firm visited the customer filing the complaint and repaired the pumps demonstrating the problem. The firm will correct other units as complaints are received. The firm modified its recall strategy and issued a Device Correction Letter dated 6/22/07 notifying all users of the problem
Quantity728 pumps of all models
DistributionWorldwide: USA and Bangladesh, Belgium, Bolivia, Canada, Chile, Colombia, Costa Rica, Egypt, Equador, Hong Kong, India, Indonesia, Japan, Latin America, Malaysia, Nicaragua, Philippines, Saudi Arabia, Taipe, Taiwan, United Arab Emirates, Uruguay, and Viet Nam.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K915183SARNS 8000 MODULAR PERFUSION SYSTEM
3M Health Care, Sarns, Jul 8, 1992
K953904SARNS 9000 UNIVERSAL ROLLER PUMP
3M Health Care, Ltd., Apr 19, 1996