Product group Injections / Infusions / Transfusions / Dialysis
Reference 01487/06

The company ProRhythm, Inc. has issued a recall notification for the Transseptal Sheath, 16.5F with Dilator due to a possible delamination of tip bonding during a procedure with the HIFU Ablation System.

Recall of the Transseptal Sheath, 16.5F with Dilator from ProRhythm , Download_VeroeffentlichtAm_EN 2006.07.03 PDF, 22KB, File does not meet accessibility standards