Herceptin (Haemato Pharm)
Recall
|
Medicines
|
16/04/2014
The distribution company informed its supplied customers on 04/16/2014 and asked for a stock check of the affected batch.
Name of the medicinal product | Herceptin 150 mg Pulver zur Herstellung eines Infusionslösungskonzentrats |
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Marketing authorisation number(s) | EU/1/00/145/001 |
Marketing authorisation holder | Roche Registration Limited Paralleldistribution: HAEMATO PHARM GmbH Vertrieb und Durchführung Rückruf: AXELERIS Pharma GmbH |
Batch number(s) | H4196B01 |
Classification of the recall | 2 |
BASG reference number | INS - 640.001 - 108 6 |
Further inquiry note
Page last modified:
12/07/2022