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Lydaxx 100mg/ml solution recalled over sterility concerns
The recall affects a single batch of Lydaxx 100mg/ml solution for cattle, pigs and sheep.
Product may be compromised owing to crimping of the aluminium cap.

The Veterinary Medicines Directorate (VMD) has issued a product defect recall alert for Lydaxx 100mg/ml solution for cattle, pigs and sheep following sterility concerns.

The recall affects a single batch of the product -
Batch No.0C3829 Expiry Date 03/12/2022 - manufactured by Vetoquinol UK Ltd.

The recall states: “We wish to make wholesalers and veterinary surgeons aware that Vetoquinol UK Ltd has initiated a Class I recall of Lydaxx 100 mg/ml solution for injection for cattle, pigs and sheep as a precautionary measure.

“Vetoquinol have identified that there is a potential for the sterility/stability of the product to be compromised due to a crimping problem of the aluminium cap. This recall is for the 100 ml bottles of the following batch only: Batch No.0C3829 Expiry Date 03/12/2022."

Veterinary surgeons and wholesale dealers are being contacted by Vetoquinol UK Ltd to examine their inventory immediately and quarantine products subject to this recall.

More information about the recall can be obtained from Vetoquinol’s Customer Services Department on +44 1280 814500 Option 1 or email: UK_office@vetoquinol.com

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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.