Recall FlexCath®, CryoCath
2008.05.29
Product group Injections / Infusions / Transfusions / Dialysis
Reference 01739/08
CryoCath Technologies Inc. recalls all FlexCath® Steerable Sheaths of the product code 2FC12 from the market. The affected sheaths may contain macroscopic filaments which could dislodge from the assembly and possibly enter the bloodstream during use.