Recall FlexCath®, CryoCath
2008.05.29
Product group Injections / Infusions / Transfusions / Dialysis
Reference 01786/08
CryoCath Technologies Inc. recalls all FlexCath® Steerable Sheaths of the product code 3FC12 from the market. The affected sheaths may contain excess plastic material in the stop cock of the side flush port which could dislodge from the assembly and possibly enter the bloodstream during use.