Nerfasin
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 |
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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 recall | 1 |
BASG reference number | INS-640.001-1295 |
Further inquiry note
Page last modified:
12/07/2022