Typhim-Vi
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 recall | 2 |
| BASG reference number | INS-640.001-0542 |
Further inquiry note
Page last modified:
12/07/2022