In accordance with Article 152 of Regulation (EU) 2019/6, all marketing authorisations for veterinary medicinal products (VMPs) granted under Directive 2001/82/EC, as amended, must be updated to align their product information with QRD template version 9.These updates must be completed at the latest by 29 January 2027, after which all products placed on the market must have product information compliant with QRD v9.

Recall due to deviations from quality standards at the production site

Recall due to deviations from quality standards at the production site

Recall due to deviations from quality standards at the production site

Recall due to deviations from quality standards at the production site

Recall due to deviations from quality standards at the production site

Recall due to possible particles in solution

Recall due to particles in the solvent

Recall due to deviations from quality standards at the production site

Recall due to deviations from quality standards at the production site