Axura
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 underdosage) has been detected in dosing pumps in the prepackages of Axura 5 mg/pump stroke, 50 ml solution for oral use. Therefore, the affected batches are recalled by wholesalers, pharmacies as well as physicians (physician samples).
| Name of the medicinal product | Axura 5mg/Pumpenhub, Lösung zum Einnehmen |
|---|---|
| Marketing authorisation number(s) | EU/1/02/218/005 - 006, 011 |
| Marketing authorisation holder | Merz Pharmaceuticals GmbH Vertrieb & Durchführung Rückruf: Merz Pharma Austria GmbH |
| Batch number(s) | 362385, 363808, 365952, 367181, 368181, 370793, 471657, 473619, 475446 Ärztemusterchargen: 368182, 369511, 472323 |
| Classification of the recall | 2 |
| BASG reference number | INS - 640.001 - 1292 |
Further inquiry note
Page last modified:
12/07/2022