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.

Recall FlexCath®, CryoCath , Download_VeroeffentlichtAm_EN 2008.05.29 PDF, 64KB, File does not meet accessibility standards