BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall of PENTARAY catheters, Johnson & Johnson Medical NV/SA / Biosense Webster

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 03231/16

For further information as well as details concerning the device please see the enclosed Advisory Notice of the manufacturer.

Recall of PENTARAY catheters, Johnson & Johnson Medical NV/SA / Biosense Webster , Download_VeroeffentlichtAm_EN PDF, 300KB, File does not meet accessibility standards