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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall Prolene Mesh General and Plastic Surgery Devices Cardinal Health 2 United States USFDA
Device Recall S.M.A.R.T. CONTROL Transhepatic Biliary Stent Gastroenterology-Urology Devices Cordis Corporation 2 United States USFDA
FLEXSTENT Biliary SelfExpanding Stent System (US Commercial 120 cm Length) Gastroenterology-Urology Devices Cordis Corporation 2 United States USFDA
FLEXSTENT Biliary SelfExpanding Stent System (US Commercial 80 cm Length) Gastroenterology-Urology Devices Cordis Corporation 2 United States USFDA
Device Recall PRECISE RX Gastroenterology-Urology Devices Cordis Corporation 2 United States USFDA
Transhepatic Biliary Stent System Gastroenterology-Urology Devices Cordis Corporation 2 United States USFDA
Transhepatic Biliary Stent System Gastroenterology-Urology Devices Cordis Corporation 2 United States USFDA
Device Recall S.M.A.R.T. Flex Biliary/Vascular selfexpanding stent system Gastroenterology-Urology Devices Cordis Corporation 2 United States USFDA
Device Recall CORDIS S.M.A.R.T. Control" Nitinol Stent System Cardiovascular Devices Cordis Corporation 3 United States USFDA
Device Recall Cordis PRECIS (R) Rx Nitinol Stent System Cardiovascular Devices Cordis Corporation 3 United States USFDA
Device Recall Cordis S.M.A.R.T. Flex Vascular Stent System Cardiovascular Devices Cordis Corporation 3 United States USFDA
Cypher Sirolimus-eluting Coronary Stent on Raptor Over-the-Wire Delivery System (CWSxxxxx), and Cypher RX Sirolimus-eluting Coronary Stent on RaptorRail Rapid Exchange Delivery System CXSxxxxx Cardiovascular Devices Cordis Corporation 3 United States USFDA
Device Recall Cypher sterile stent Cardiovascular Devices Cordis Corporation 3 United States USFDA
the OPTEASE® Retrievable Vena Cava Filter Cardiovascular Devices Cordis Germany BAM
OPTEASE temporary vena cava filter Cardiovascular Devices Cordis Cashel Sweden SMPA
Device Recall S.M.A.R.T. CONTROL NITINOL STENT SYSTEM ILIAC Cardiovascular Devices Cordis Corporation 3 United States USFDA
Device Recall OptEase Vena Cava Filter Cardiovascular Devices Cordis Corporation 2 United States USFDA
Device Recall Cordis PRECIS (R) PRO Rx Nitinol Stent System Cardiovascular Devices Cordis Corporation 3 United States USFDA
FLEXSTENT Femoropopliteal SelfExpanding Stent System (Clinical Study Protocol FSS0003 (OPEN trial) Cardiovascular Devices Cordis Corporation 3 United States USFDA
FLEXSTENT Femoropopliteal SelfExpanding Stent System (EU Commercial 80 cm Length) Cardiovascular Devices Cordis Corporation 3 United States USFDA
FLEXSTENT Femoropopliteal SelfExpanding Stent System (EU Commercial 120 cm Length) Cardiovascular Devices Cordis Corporation 3 United States USFDA
Cordis OPTEASE Vena Cava Filter Cardiovascular Devices Cordis Corporation 2 United States USFDA
all unexpired lots of „S.M.A.R.T. CONTROL“ Nitinol Stent System Cordis Germany BAM
affected lots of the coronay stent “Cypher Select ™+“ Cordis Germany BAM
Cypher Select® + Sirolimus-eluting Coronary Stents Cordis Germany BAM