BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Lot Recall of Aortic Cannulae and Retrograde Cardioplegia Cannulae, Sorin Group

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 04535/13

Sorin Group informs about the recall of 5 lot numbers of Aortic Cannulae and Retrograde Cardioplegia Cannulae, because these devices are not labelled in compliance with the Medical Devices Directive.

Lot Recall of Aortic Cannulae and Retrograde Cardioplegia Cannulae, Sorin Group , Download_VeroeffentlichtAm_EN PDF, 129KB, File does not meet accessibility standards