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BSE detected in US dairy cow
USDA confirms fourth US case

Officials of the United States Department of Agriculture (USDA) have confirmed that a single dairy cow in California has tested positive for bovine spongiform encephalopathy (BSE). The USDA also confirmed that the animal died on a farm in central California before it could be presented for slaughter and therefore never reached either the food or feed chains. Consequently, there has been no risk to human health.

It is understood that the cow was first noticed to be nonambulatory (colloquially, a 'downer') at the farm of origin, and the carcass is currently being held at a rendering facility under the authority of the State of California prior to its destruction. Western Blot tests and immunohistochemistry have established that the cow had atypical BSE, an exceptionally rare variant of the disease not usually associated with the consumption of infected feed but instead acquired spontaneously.

Commenting, USDA Chief Veterinary Officer John Clifford has emphasized that "This detection in no way affects the United States' BSE status as determined by the OIE [World Animal Health]. The United States has in place all of the elements of a system that OIE has determined ensures that beef and beef products are safe for human consumption: a mammalian feed ban, removal of specified risk materials, and vigorous surveillance. Consequently, this detection should not affect U.S. Trade." 

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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.