The marketing authorisation holder informed its customers on December 29, 2022, that glass splinters were found in individual bottles of the batch of bottles used. For this reason, the batch in question is recalled as a precautionary measure.
|Name of the medicinal product||BRONCHOSTOP Erkältungssaft|
|Marketing authorisation number(s)||739029|
|Marketing authorisation holder||Kwizda Pharma GmbH|
|Classification of the recall||1|
|Depth of recall||Patients|
|BASG reference number||INS-640.001-4136|
|Safety warnings Link||Safety information on the quality defect/recall „BRONCHOSTOP Erkältungssaft“|