Recall of Ablation Catheters HIFU-ST01-25 and HIFU-ST01-30 from ProRhythm
2006.08.11
Product group Injections / Infusions / Transfusions / Dialysis
Reference 01503/06
The company ProRhythm, Inc. has issued an information concerning a recall of Ablation Catheters HIFU-ST01-25 and HIFU-ST01-30. The depth of lesion could possibly extend beyond myocardium and cause unwanted damage of adjacent tissue.