Edwards Lifesciences Research Medical Inc
West Midvale, UT
This page shows every FDA and USDA recall linked to Edwards Lifesciences Research Medical Inc. Each entry includes the product involved, when the recall happened, and how serious it was. If a company has had multiple recalls over the years, you can see the full history here in one place — including whether any were Class I, which is the most serious type.
10
Total Recalls
2004
First Recall
2009
Most Recent
EndoClamp aortic catheter label reading in part: "CARDIOVATIONS EndoClamp aortic catheter 65 cm,STERILE R, REF...
Nov 6, 2009
· Device
Terminated
EndoClamp aortic catheter. Label reading in part: "***CARDIOVATIONS EndoClamp aortic catheter 100 cm, REF EC10...
Nov 6, 2009
· Device
Terminated
Edwards Lifesciences CardioVations, EndoClamp aortic catheter 100 cm, REF EC1001, Sterile R, individually pack...
Jan 5, 2009
· Device
Terminated
CardioVations Ethicon, a Johnson and Johnson company, EndoClamp aortic catheter 100 cm, REF EC1001, Sterile R,...
Jan 5, 2009
· Device
Terminated
Thin-Flex Venous Return Cannulae with Duraflo coating, REF DTF3343O, 33/43 Fr. x 39 cm, Sterile EO, Edwards Li...
Sep 26, 2008
· Device
Terminated
Thin-Flex Venous Return Cannulae, 33/43 FR. x 39 cm, REF TF3343O, Sterile EO, Edwards Lifesciences LLC, Irvine...
Sep 26, 2008
· Device
Terminated
Thin-Flex Venous Return Cannulae, 33/43 Fr. x 39 cm, REF TF3343OA, Sterile EO, Edwards Lifesciences LLC, Irvin...
Sep 26, 2008
· Device
Terminated
Edwards Lifesciences LLC, Fem-Flex II Femoral Venous Cannula, 12 Fr. x 11.5 cm, REF FEMII012V, Cardiopulmonary...
Sep 11, 2008
· Device
Terminated
Edwards Lifesciences LLC, Fem-Flex II Duraflo Treated Femoral Venous Catheter, 8 Fr. x 11.5 cm, REF DIIFEMII00...
Sep 11, 2008
· Device
Terminated
EMBOL-X Slim Access Device / Aortic Cannula 24 Fr X 11''.
Dec 15, 2004
· Device
Terminated