GovWire

Guidance: Report a product defect: veterinary medicine

Veterinary Medicines Directorate

January 9
10:14 2023

Reporting a product defect

If a pharmaceutical company becomes aware of an issue or defect with one of their products or a batch of product they must report this to the Veterinary Medicines Directorate (VMD).

Complete the Product defect report form (ODT, 38.6 KB) and send it to rapidalert@vmd.gov.uk.

If the product or batch is likely to be recalled due to the defect you must contact the VMD to discuss the issue. Where appropriate give details of the level of recall, for example wholesaler level, veterinary practice level.

All other reporters should contact the marketing authorisation holder.

Do not use this form to report an adverse event to a veterinary medicine or microchip; To report a suspected adverse event.

List of recalled products

Products recalled in the UK in the last 12 months.

Product Notification Date Batch No. Level of Recall Problem
Product defect recall alert for Anesketin 100 mg/ml solution for injection for dogs, cats and horses 06/01/2023 140461 Vet Level This recall is due to a compromised closure of the vials
Nerfasin 20 mg/ml Solution for Injection for Cattle, Horses, Dogs and Cats Product defect recall alert 18/07/22 All batches on the market Vet Level This recall is due to particulate matter found in retained samples that were previously particle free

What issues are classed as a product defect

These include:

  • incorrect labelling, such as product strength, name of ingredients
  • misinformation or lack of information on the packaging or leaflets
  • incorrect manufacture, such as strength of the ingredients or an issue with the container
  • contamination of any kind
  • stability, such as expiry
  • counterfeit or deliberately tampered with product

Further information on how the VMD handles product defect reports.

The holder of an authorisation referred to in Article 44 of Directive 2001/82/EC (for veterinary products) is required by Article 13 of Directive 91/412/EEC (for veterinary products) to implement an effective procedure for the recall of defective products. The authorisation holder is required to notify the relevant Competent Authority of any defect that could result in a recall and indicate, as far as possible, the countries of destination of the defective product.

For information on human medicines please visit the MHRA Safety Information page.

Contact

rapidalert@vmd.gov.uk

Alternatively phone the Inspections team via the switchboard on, 01932 336911.

Published 17 November 2014
Last updated 9 January 2023 +show all updates
  1. Product recall list for last 12 months updated

  2. Update to table of recalled products

  3. Update table of recalled products

  4. Updated table of recalled products: Lydaxx 100 mg/ml solution for injection for cattle, pigs and sheep Ketofen 10% Solution for Injection

  5. Salmovac 440 added to list of recalled products

  6. Product defect recall alert added for Prid Delta 1.55 g Vaginal Delivery System for Cattle.

  7. Updated to include January 2021 notices

  8. Table of recalled products updated

  9. Updated table of recalled products

  10. Added Johnsons 4Fleas 80mg Spot-on Solution for Cats to table of recalled products

  11. Added Foston 20% w/v Solution for Injection - Product defect recall alert

  12. Updated table of recalled products

  13. Updated table of recalled products

  14. Update to the table of recalled products - Clavubactin

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