Eumitan
Recall
|
Medicines
|
13/01/2015
The marketing authorization holder informed its supplied customers in a letter dated January 13, 2015, that the package leaflet in Greek was enclosed with individual packages of batch 42053 and that a precautionary recall is therefore being carried out.
Name of the medicinal product | Eumitan 2,5 mg -Filmtabletten |
---|---|
Marketing authorisation number(s) | 1-24486 |
Marketing authorisation holder | Menarini International Operations Luxembourg S.A. Durchführung Rückruf: A. Menarini Pharma GmbH |
Batch number(s) | 42053 |
Classification of the recall | 3 |
BASG reference number | INS-640.001-1312 |
Further inquiry note
Page last modified:
12/07/2022