The marketing authorization holder has informed its supplied customers in a letter dated August 10, 2017, that a batch of Vibravenous - Ampoules with batch number B113306 is being recalled due to distinct color changes.
|Name of the medicinal product||Vibravenös - Ampullen|
|Marketing authorisation number(s)||1 - 15051|
|Marketing authorisation holder||Pfizer Corporation Austria GmbH|
|Classification of the recall||2|
|BASG reference number||INS - 640.001 - 2160|