Recall | Veterinary Medicines | 19/12/2014

The distributor has informed its supplied customers in a letter dated 18.12.2014 that there is a possibility of incorrect labeling or batch submixing with 100 mg/ml nerfasin vials in the above batch. To date, there have only been reports of this from the French market, but a precautionary recall is being carried out in order to rule out any risk to the health of the animals.

Name of the medicinal product Nerfasin vet. 20 mg/ml - Injektionslösung für Rinder, Pferde, Hunde und Katzen
Marketing authorisation number(s) 8-01053
Marketing authorisation holder Le Vet BV

Vertrieb & Durchführung Rückruf:
Richter Pharma AG
Batch number(s) 13H026
Classification of the recall1
BASG reference number INS-640.001-1295

Further inquiry note