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VMD recalls chicken vaccine over efficacy concerns
The VMD has issued a product recall alert for a single batch of Salmovac 400.
Veterinary surgeons urged to examine their inventories immediately.

The Veterinary Medicines Directorate (VMD) has issued a product recall alert for a batch of Salmovac 440, manufactured by CEVA Animal Health, over concerns about its efficacy.

Salmovac 440 is used in chickens to protect them against Salmonella Enteritidis and Salmonella Typhimurium. Usually administered via drinking water, it contains the contains the live Salmonella Enteritidis strain in freeze-dried form. 

The VMD writes: ‘We wish to make veterinary surgeons aware that Ceva Animal Health Ltd has initiated a Class II recall to veterinary level for the product Salmovac 440.

‘Following testing Ceva Animal Health Ltd have confirmed that Batch No. 3000520B with an Expiry date of 11 December 2021 has live bacterial count values (potency) below the authorised specification and there is potential for a lack of efficacy.

‘Ceva Animal Health Ltd is contacting veterinary surgeons to examine inventory immediately and quarantine products subject to this recall.’

Further information about the recall is available from Ms Helen Houghton, poultry business unit manager, on 01494 781510. 

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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. 

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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.