Velcade
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 recall | 2 |
| BASG reference number | INS-640.001-2391 |
Further inquiry note
Page last modified:
12/07/2022