BfArM - Federal Institute for Drugs and Medical Devices

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Information on medicinal products traded illegally in Romania on the German market

Active substance: rituximab, trastuzumab

The Romanian medicines licensing authority (ANMDM) has informed the Federal Institute for Drugs and Medical Devices (BfArM) and the Paul-Ehrlich-Institut (PEI) via the European Rapid Alert System that batches of 45 medicinal products traded by the Romanian wholesale distributor Chemomed are being recalled.

risk information - full text (available in German only)