Recall | Medicines | 25/09/2012

Sanofi Pasteur MSD GmbH has informed its supplied customers in a letter dated 24.09.2012 that a voluntary recall is being carried out for the above-mentioned batches due to a possibly too low antigen content.

Name of the medicinal product Typhim Vi - Fertigspritze
Marketing authorisation number(s) 2-00093
Marketing authorisation holder Sanofi Pasteur MSD S.N.C.

Vertrieb & Durchführung Rückruf:
Sanofi Pasteur MSD GmbH
Batch number(s) G0484-3, H0048-3, H0318-2
Classification of the recall2
BASG reference number INS-640.001-0542

Further inquiry note