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VMD announces product recall
The recall has been issued due to a defect with the metal cap thread, which means re-sealed bottles may not be airtight.
Class two recall of anaesthetic products due to defect

The Veterinary Medicines Directorate (VMD) is making wholesalers and veterinary surgeons aware of a recall of certain anaesthetic products.

A class two recall has been issued regarding the following veterinary anaesthetic products, which are manufactured by Zoetis UK Limited:
  • IsoFlo 100% w/w Inhalation Vapour Liquid Vm 42058/4195
  • Isothesia 1000 mg/g Inhalation Vapour Liquid Vm 42058/4197

The recall has been issued due to a defect with the metal cap thread, which means re-sealed bottles may not be airtight. Batches with an expiry date of 31 May 2021 or later are not included in the recall.

Class two recalls indicate that the defect may cause mistreatment or harm to the patient, but is not life-threatening or serious.

The affected batches are:

IsoFlo 250ml
58006XN, 60003XN, 59005XN, 60006XN, 61001XN, 60016XN, 60017XN, 61018XN, 61015XN, 61016XN, 61017XN, 6062216, 6062225, 6062226, 6062217, 6063738

Isothesia 250ml
6062335, 6063318

For further information, contact Zoetis technical services on 0845 300 8034 or customersupportuk@zoetis.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. 

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.