Ropinaest
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 recall | 2 |
| Depth of recall | Pharmacies |
| BASG reference number | INS-640.00-2933 |
Further inquiry note
Page last modified:
07/11/2019