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Revozyn RTU 400 mg/ml Suspension for Injection for Cattle, Recall, One batch

26/03/2025
Medicines for animal use Recall

We wish to advise you that one batch of the veterinary medicine Revozyn RTU 400 mg/ml Suspension for Injection for Cattle is being recalled by Dechra Pharmaceuticals PLC.

This recall is going to veterinary level.

The recall is due to a stability failure in relation to the resuspendability parameter.

The recall letter, dated 25th March 2025, can be downloaded in the Documents section at the bottom of this webpage.

 

Product information

Active substance
Penethamate hydriodide
Authorisation holder
Eurovet Animal Health B.V.
Authorisation number
VPA10989/071/001
Serial or batch number and expiry date
Batch Number 23G043, Expiry date Jun 2025
Human or veterinary medicine
Veterinary
Target audience
Veterinary professionals
Recall level
Veterinary level

Actions to be taken

Information for veterinary professionals

Veterinarians are requested to perform the following actions:

  1. Check your current inventory and immediately quarantine any units of the batch which you have in your veterinary surgery.
  2. If you have supplied units of the batch to any other surgery, pharmacy or any other healthcare facility, please contact them and request that they return any unused units to you.
  3. Contact the wholesaler from which you purchased the stock to arrange for the return of all quarantined units using the returns form contained in the recall letter, available in the Documents section below. Please ensure the product is packed in suitable containers to avoid any damage in transit.

Replacement stock is available to order at this time.

Information for public

No action is required at user level. If you have this veterinary medication in your possession and have any queries, please contact your veterinary surgery.

 

Documents

Opens in new window Revozyn Recall - Veterinarian Letter - IE 25 MAR 2025 PDF : 106KB | 26/03/2025