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VMD issues product defect recall alert
The recall affects batches of Carprieve 5% w/v Small Animal Solution for Injection.

Recall is a precautionary measure owing to higher than usual impurities.

The Veterinary Medicines Directorate (VMD) has issued a product defect recall alert for Carprieve 5% w/v Small Animal Solution for Injection, manufactured by Norbrook Laboratories Ltd.

A statement reads: 'We wish to make veterinary surgeons aware that Norbrook Laboratories Ltd have initiated a Class 2 recall to veterinarian level for the product Carprieve 5% w/v Small Animal Solution for Injection. This is as a precautionary measure due to higher than usual impurities.

'A health hazard assessment has been completed by the company veterinary surgeon. This concludes that any risk to animal and human health is likely to be low and no greater than expected for this product under normal conditions, as described on the product labelling.'

The recall affects the following batch numbers:

0265-90 
0302-90 
0246-90 
0112-90 
0295-90 
9053-91 
9103-91

The statement continues: 'Norbrook Laboratories Ltd are contacting veterinary surgeons to examine inventory immediately and quarantine products subject to this recall.'

For further information regarding the recall contact Gary Mckee on +44 2830 264435 or email gary.mckee@norbrook.co.uk 

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FIVP launches CMA remedies survey

News Story 1
 FIVP has shared a survey, inviting those working in independent practice to share their views on the CMA's proposed remedies.

The Impact Assessment will help inform the group's response to the CMA, as it prepares to submit further evidence to the Inquiry Group. FIVP will also be attending a hearing in November.

Data will be anonymised and used solely for FIVP's response to the CMA. The survey will close on Friday, 31 October 2025. 

Click here for more...
News Shorts
CMA to host webinar exploring provisional decisions

The Competition and Markets Authority (CMA) is to host a webinar for veterinary professionals to explain the details of its provisional decisions, released on 15 October 2025.

The webinar will take place on Wednesday, 29 October 2025 from 1.00pm to 2.00pm.

Officials will discuss the changes which those in practice may need to make if the provisional remedies go ahead. They will also share what happens next with the investigation.

The CMA will be answering questions from the main parties of the investigation, as well as other questions submitted ahead of the webinar.

Attendees can register here before Wednesday, 29 October at 11am. Questions must be submitted before 10am on 27 October.

A recording of the webinar will be accessible after the event.