Yondelis
Recall
|
Medicines
|
02/04/2015
The distribution company informed its supplied customers by letter dated 01.04.2015 that various finished product batches from a single bulk are being recalled because black visible particles were detected.
| Name of the medicinal product | Yondelis 0,25 mg Pulver zur Herstellung eines Infusionslösungskonzentrats |
|---|---|
| Marketing authorisation number(s) | EU/1/07/417/001 |
| Marketing authorisation holder | Pharma Mar, S.A. Vertrieb und Durchführung Rückruf: Idis Pharma |
| Batch number(s) | Österreich: 14116, 14135, 15001 Alle Chargen, die aus dem betroffenen Bulk hergestellt wurden: 14113, 14116, 14117, 14130, 14131, 14134, 14135, 14136, 14148, 14150, 14152, 14159, 14160, 14161, 15001, 15002, 15004, 15011, 15025 |
| Classification of the recall | 1 |
| BASG reference number | INS-640.001-1375 |
Further inquiry note
Page last modified:
12/07/2022