Yondelis
Recall
|
Medicines
|
23/06/2016
The marketing authorization holder informed its supplied customers in a letter dated June 20, 2016, that a precautionary recall is being carried out due to the potential risk of glass particles in the vials.
| Name of the medicinal product | Yondelis 0,25 mg Pulver zur Herstellung eines Infusionslösungskonzentrats |
|---|---|
| Marketing authorisation number(s) | EU/1/07/417/001 |
| Marketing authorisation holder | PharmaMar S.A. |
| Batch number(s) | 16013, 16015, 16033 |
| Classification of the recall | 1 |
| BASG reference number | INS - 640.001 - 1757 - 010 |
Further inquiry note
Page last modified:
12/07/2022