ClearanceBrief
Recall Z-0542-2011 ยท DTL Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass

Edwards Lifesciences Llc

Edwards Protection Cannulae - Monitoring and Infusion Set, Model ISP3147, Sterile EO, Edwards Lifesciences LLC, One Edwards Way, Irvine, CA 92614

DateDec 7, 2010 (initiated Oct 19, 2010)
StatusTerminated
ReasonMonitoring and Infusion Set connectors may break during manipulation.
Root causeEmployee error
ActionEdwards Lifesciences issued a Urgent Product Recall letter dated October 13, 2010 to customers identifying the affected devices, requesting the return of unused devices and completion and return of a response form. Further information is available at 800-424-3278.
Quantity322 sets
DistributionNationwide Distribution: in the states of FL, KS, MO, TX, VA, and PR.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K892377RMI AORTIC ROOT/CORONARY SINUS MONIT./INFUSION SET
Research Medical, Inc., Dec 7, 1989