Limaxetin
Recall
|
Medicines
|
12/06/2018
The marketing authorization holder has informed its supplied customers in a letter dated 11.06.2018 that visible particles were found in part of a production batch during quality control. For this reason, the above batch is being recalled as a precautionary measure.
| Name of the medicinal product | LiMAxetin 4 mg/ml Injektionslösung |
|---|---|
| Marketing authorisation number(s) | 138125 |
| Marketing authorisation holder | Humedics GmbH |
| Batch number(s) | 2018AT01/A |
| Classification of the recall | 1 |
| BASG reference number | INS-640.001-2558 |
Further inquiry note
Page last modified:
12/07/2022