ClearanceBrief
Recall Z-2348-2012 ยท DTQ Console, Heart-Lung Machine, Cardiopulmonary Bypass

Terumo Cardiovascular Systems Corporation

Safety monitor included with System 8000 Base The Sarns" Modular Perfusion System 8000 is indicated for use for up to 6 hours on the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, when used by a qualified medical professional who is experienced in the operation of this or similar equipment. The safety monitor is indicated to

DateSep 11, 2012 (initiated Aug 12, 2009)
StatusTerminated
ReasonTerumo Cardiovascular Systems (Terumo CVS) received complaints from our Affiliate, Terumo Dubai that the safety monitors were tripping off. Terumo CVS' investigation determined that 8 monitors were manufactured with an underrated circuit breaker due to an error where an associate pulled an underrated circuit breaker from an incorrect inventory location. Since this time, inventory locations hav
Root causeMixed-up of materials/components
ActionTERUMO Cardiovascular Systems communicated with their affiliate, Terumo Dubai, in 2009 at the time the complaints were reported. No further communication was warranted. For questions regarding this recall call 734-741-6173.
Quantity8
DistributionWorldwide distribution: International only-country of: Terumo Dubai, UAE
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K915183SARNS 8000 MODULAR PERFUSION SYSTEM
3M Health Care, Sarns, Jul 8, 1992