Ebixa
Recall
|
Medicines
|
17/12/2014
The distribution company has informed its supplied customers in a letter dated December 16, 2014, that in individual cases a dosage inaccuracy (slight underdosing) has been detected in dosing pumps in the prepackages of Ebixa5 mg/pump hub, 50 ml solution for oral use. Therefore, the affected batches are recalled.
| Name of the medicinal product | Ebixa 5 mg/Pumpenhub, Lösung zum Einnehmen |
|---|---|
| Marketing authorisation number(s) | EU/1/02/219/005-006, 013 |
| Marketing authorisation holder | H. Lundbeck A/S Vertrieb & Durchführung Rückruf: Lundbeck Austria GmH |
| Batch number(s) | 365770, 370334, 474208 |
| Classification of the recall | 2 |
| BASG reference number | INS - 640.001 - 1293 |
Further inquiry note
Page last modified:
12/07/2022