Your data on MRCVSonline
The nature of the services provided by Vision Media means that we might obtain certain information about you.
Please read our Data Protection and Privacy Policy for details.

In addition, (with your consent) some parts of our website may store a 'cookie' in your browser for the purposes of
functionality or performance monitoring.
Click here to manage your settings.
If you would like to forward this story on to a friend, simply fill in the form below and click send.

Your friend's email:
Your email:
Your name:
 
 
Send Cancel

Risk of microchip problems 'likely to be very low'
dog being scanned
The majority of reports involved microchip migration.
VMD publishes first report on adverse events

The risk of animals having an adverse reaction to microchipping is thought to be 'very low', according to a new report by the Veterinary Medicines Directorate (VMD).

Changes in the law made it a legal requirement to report microchip problems in dogs from February 2015 in England, and April 2016 in Scotland and Wales.

The VMD received 1,420 reports of adverse microchip events between April 2014, when it first launched its reporting scheme, and December 2015. Of these, most related to dogs (84.2 per cent) and the majority involved cases of microchip migration (729), followed by microchip failure (630) and adverse reactions (61).

Sales information for microchips is not currently available, meaning it is impossible to calculate the risk of an adverse reaction from these figures. However considering there are an estimated 8.5 million dogs and 7.5 million cats in the UK, combined with the low number of reported adverse events - despite high uptake of dog microchipping in 2015 - the VMD believes the likelihood is 'very low'.

An adverse reaction is defined as any unwanted signs or symptoms following microchipping. Of the 61 cases reported, reactions included lumps, masses or swellings at the implant site; calcification on or near the site of the microchip; discharge from abscesses and other swellings; infections at the implant site; and removal or loss of the chip. There were also a few reports of equipment problems and some that included details of vaccinations given either before or at the same time as the chip was implanted.

Chip failure is when a microchip has not been found after a full body scan with a working scanner. Although there were 630 such reports, the VMD says only 56 of these can be considered true failures, as the presence of the chip was not confirmed in the other cases.

Out of the 729 reports of migration (where the chip has moved a significant distance from the implant site), nearly 300 cases were unlikely to be migrations, according to the report, as the chip was still within the neck/scapula/shoulder area. In total, 302 reports appear to be true migrations.

There was a variety of missing information in the reports received. The confusion in supplying the required information is 'no surprise', the VMD wrote, as there are such a large number of microchip manufacturers, brand names, implanter organisations and databases. Efforts are being made to improve the reporting form to make it easier to complete.

In the next year, the VMD will provide clearer guidance, which it hopes will reduce the number of 'unlikely' migration reports. It also plans to collect sales details from each of the manufacturers to improve interoperation of the results.

Become a member or log in to add this story to your CPD history

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.