Hexyon Injektionssuspension in einer Fertigspritze
The marketing authorisation holder/local representative informed its customers on November 17, 2022, that in two packs of "Hexyon" (batch: U3P166V – 6-fold vaccine for Austria) one syringe of "Tetraxim" (batch: V3B791V – 4-fold vaccine for Poland and Romania) was identified by the administering physicians before use. For this reason, this batch is recalled.
|Name of the medicinal product||Hexyon Injektionssuspension in einer Fertigspritze|
|Marketing authorisation number(s)||EU/1/13/829/007|
|Marketing authorisation holder||Sanofi Pasteur Europe|
|Classification of the recall||2|
|Depth of recall||Pharmacies|
|BASG reference number||INS-640.001-4043|