Veterinary Medicines | 25/07/2012

The marketing authorization holder has informed its supplied customers in a letter dated July 25, 2012, that the folding box of batch 1261105 is incorrectly labeled "For intramuscular injection", but the product is injected subcutaneously. Therefore, a recall is being implemented as a precautionary measure.

Name of the medicinal product RESFLOR, 300/16,5 mg/ml Injektionslösung für Rinde
Marketing authorisation number(s) 8-00707
Marketing authorisation holder Intervet GmbH, Austria
Batch number(s) 1261105
Classification of the recall2
BASG reference number INS-640.001-0489

Further inquiry note