Binocrit Injektionslösung in einer Fertigspritze

Recall | Medicines | 30/09/2020

The parallel distributor - „Orifarm GmbH“ - informed its customers on September 30, 2020 that stability testing showed a deviation, which may result in a reduced efficacy.

So the affected batches are recalled precautionary.

Name of the medicinal product 1) Binocrit 30.000 I.E./0,75 ml Injektionslösung in einer Fertigspritze
2) Binocrit 40.000 I.E./1 ml Injektionslösung in einer Fertigspritze
Marketing authorisation number(s) 1) EU/1/07/410/054
2) EU/1/07/410/055
CIP code 1) 4973188
2) 4973194
Marketing authorisation holder Sandoz GmbH

Paralleldistribution:
Orifarm GmbH
Batch number(s) 1) 2004080022
2) 1912050066, 2001300049, 2002140001, 2002190068
Classification of the recall 2
Depth of recall Pharmacies
BASG reference number INS-640.001-3332
Email

Further inquiry note