BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall for Omniflush, B. Braun Melsungen AG

Product group Physical therapy
Reference 01180/11

The manufacturer B. Braun Melsungen AG informs about a recall of batches of Omniflush Syringes, prefilled with 0,9% sodium chloride solution, because the labelling concerning the sterilisation method is not correct.

Recall for Omniflush, B. Braun Melsungen AG , Download_VeroeffentlichtAm_EN PDF, 165KB, File does not meet accessibility standards