Recall | Medicines | 01/08/2019

The marketing authorisation holder informed its customers on August 1, 2019 that the outer packaging may leak. As sterility cannot be assured, below mentioned batch is recalled as a precautionary measure.

Name of the medicinal product Ropinaest 2 mg/ml - Infusionslösung
Marketing authorisation number(s) 1-30929
Marketing authorisation holder Gebro Pharma GmbH
Batch number(s) 435219
Classification of the recall2
Depth of recall Pharmacies
BASG reference number INS-640.00-2933

Further inquiry note