Velactis
Recall
|
Veterinary Medicines
|
26/07/2016
The marketing authorization holder has informed its supplied customers that a recall of all batches of "Velactis" on the market will be carried out, as serious side effects have been reported since market launch. The Scientific Committee for Medicinal Products for Veterinary Use of the European Medicines Agency (EMA) has therefore decided to recommend to the European Commission that the marketing authorization be suspended.
| Name of the medicinal product | Velactis 1,12 mg/ml Injektionslösung für Rinder |
|---|---|
| Marketing authorisation number(s) | EU/2/15/192/001-004 |
| Marketing authorisation holder | Ceva Santé Animale |
| Batch number(s) | 106A3, 107A2 |
| Classification of the recall | Nicht anwendar (Rückruf aufgrund von schwerwiegenden Nebenwirkungen) |
| BASG reference number | INS-640.001-1783 |
| Safety warnings Link | http://www.basg.gv.at/arzneimittel/veterinaerarznei |
| Further information Link | http://www.ema.europa.eu/ema/index.jsp?curl=pages/n |
Further inquiry note
Page last modified:
12/07/2022