Recall | Medicines | 07/02/2018

The marketing authorization holder has informed its supplied customers in a letter dated 06.02.2018 that complaints about loose or rotating metal caps have been received. Therefore, the affected batches are recalled from the market as a precaution.

Name of the medicinal product VELCADE 3,5 mg Pulver zur Herstellung einer Injektionslösung
Marketing authorisation number(s) EU/1/04/274/001
Marketing authorisation holder Janssen-Cilag International NV
Batch number(s) GJZT700, GJZTA00, GLZSM00
Classification of the recall2
BASG reference number INS-640.001-2391

Further inquiry note