MHRA Welcomes Sentencing in Medical Device Fraud Convictions

We use some essential cookies to make this website work. We’d like to set additional cookies to understand how you use GOV.UK, remember your settings and improve government services. We also use cookies set by other sites to help us deliver content from their services. You have accepted additional cookies. You can change your cookie settings at any time. You have rejected additional cookies. You can change your cookie settings at any time. Following convictions related to falsely certified medical devices, the MHRA has welcomed the sentencing in a long-running enforcement investigation. The Medicines and Healthcare products Regulatory Agency (MHRA) has welcomed the sentencing of Kenneth George Harrison following a long-running investigation into the illegal supply of medical devices used in hospitals across the UK. At Manchester Crown Court yesterday (23 September 2026), Kenneth George Harrison, aged 70, of Bolton, received a concurrent sentence for all counts, resulting in a three-year prison sentence suspended for three years. He was also ordered to complete 175 hours of community service, 10 days of rehabilitation and has been disqualified from being a company director for eight years. The convictions, announced in July , followed a complex investigation led by the MHRA’s Devices Compliance Unit, which first identified concerns in 2013 and pursued the case for more than a decade. The investigation found that a number of devices, including enteral feeding pumps, gastrostomy button devices and blunt fill needles, were supplied with CE marking that were not valid, giving healthcare providers false assurances that the devices met the necessary safety standards. “This has been a long and complex investigation, and we’re glad to have a conclusion with today’s sentencing. It demonstrates our commitment to taking robust enforcement action against those who try to bypass regulations that help keep patients safe. “Healthcare professionals need to be able to trust that the medical devices they use have been properly assessed and meet the standards designed to protect patients. “I want to thank our MHRA investigators for their dedication and persistence over many years, as well as our partners at the Crown Prosecution Service for helping bring this case to court.” “The actions of Harrison and Medicina Limited were completely dishonest and they made substantial sales from their fraudulently labelled products. “CPS lawyers worked closely with the MHRA to prosecute this case, and we will continue to bring those who commit fraud to justice. “We have also commenced confiscation proceedings under the Proceeds of Crime Act to recover any available funds from this criminal activity.” Throughout the investigation, the MHRA took action to protect patients, including issuing safety alerts, overseeing recalls and instructing the company to stop further supply of the devices. The enteral feeding pumps were used in neonatal intensive care units and special care baby units to feed very sick newborn babies directly into their stomachs. The affected enteral feeding pumps were ultimately removed from the UK and EU markets. On 1 July 2026, Kenneth George Harrison and Medicina Limited were found guilty of fraud offences relating to P900 enteral feeding pumps, gastrostomy button devices and blunt fill needle devices. A date is yet to be fixed for Medicina Ltd sentencing. All medical devices placed on the UK market must hold a valid UKCA or CE mark. More information on regulation of medical devices in the UK can be found here . The Medicines and Healthcare products Regulatory Agency (MHRA) is responsible for regulating all medicines and medical devices in the UK by ensuring they work and are acceptably safe. All our work is underpinned by robust and fact-based judgements to ensure that the benefits justify any risks. The MHRA is an executive agency of the Department of Health and Social Care (DHSC). For media enquiries, please contact newscentre@mhra.gov.uk