Binocrit Injektionslösung in einer Fertigspritze
Recall
|
Medicines
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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 |
Further inquiry note
Page last modified:
30/09/2020