Cordis Corporation recalls Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 53
Recalled Product
Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 532-598A
Hazard / Issue
Cordis has identified that the SUPER TORQUE MB Angiographic Catheter (with Marker Bands) are being used in a manner that may allow entrapment of the catheter between endovascular devices and the vessel wall, which can lead to marker band movement or dislodgement.
Issued by
FDA
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