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 recall1
BASG reference number INS - 640.001 - 1757 - 010

Further inquiry note