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 recall2
BASG reference number INS - 640.001 - 1293

Further inquiry note