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Product recall for Clindacutin Ointment
Dechra Regulatory B.V has issued a class III recall to the wholesale level.

The product has been manufactured according to the specifications of Dutch marketing authorisation.

The Veterinary Medicines Directorate (VMD) has issued a product defect recall for all in-date batches of Clindacutin Ointment 10mg/g.

In a news release, the VMD writes: “We wish to make wholesalers and distributors aware that all in-date batches of Clindacutin Ointment 10 mg/g (Vm 50406/4011) are being recalled with immediate effect.

“Dechra Regulatory B.V has issued a class III recall to the wholesale level.

“The reason for the recall is that the product has been manufactured released according to specifications of the Dutch marketing authorisation which is not approved in this country.” 

The recall is for the following batches only BC (21H258) expiry date July 2023, and BB (21H244) expiry date July 2023.

Dechra Regulatory B.V is contacting wholesale dealers to examine inventory immediately and quarantine any products subject to recall. 

For more information please contact quality@dechra.com or externalnetwork.qa@dechra.com 

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Vets launch new podcast for pet owners

News Story 1
 Two independent vets have launched a podcast to help owners strengthen their bond with pets. Dr Maggie Roberts and Dr Vanessa Howie, who have worked in both veterinary practice and major charities, are keen to use their experience to enable people to give pets a better life.

The venture, called Vets Talking Pets, provides advice and information on a range of topics, including how to select a suitable pet, where to obtain them and how to get the best out of your vet. Maggie and Vanessa will also discuss sensitive subjects, including end-of-life care, raw food diets and the cost of veterinary care.

The podcast can be found on all the usual podcast sites, including Podbean, Apple, Amazon Music and YouTube. 

Click here for more...
News Shorts
VMD issues guidance on AVM-GSL packaging

The Veterinary Medicines Directorate (VMD) has shared advice on its requirements for medicines considered AVM-GSL.

The guidance explains the information that should be on the outer package, and sets out the typical maximum pack size for an AVM-GSL product. It also describes the user-friendly language, structure and phrases required on packaging and product leaflets.

AVM-GSL products do not require discussion between the purchaser and a veterinary professional. This means that clear product information is needed to support sales choices.

The information will be useful for submitting new products to the AVM-GSL category and lowering the distribution category of products from NFA-VPS to AVM-GSL.

The VMD's guidance can be accessed here.