IKERVIS 1 mg/ml Augentropfen, Emulsion
Recall | Medicines | 08/04/2020
The marketing authorisation holder informed its customers on April 08, 2020 that the appearance of the emulsion of mentioned batch could be colourless instead of milky white.
For this reason, this batch is recalled as a precautionary measure.
|Name of the medicinal product||IKERVIS 1 mg/ml Augentropfen, Emulsion|
|Marketing authorisation number(s)||EU/1/15/990/001-002|
|Marketing authorisation holder||Santen Oy|
|Classification of the recall||2|
|Depth of recall||Pharmacies|
|BASG reference number||INS-640.001-3169|
Further inquiry note
Page last modified: 08/04/2020