MHRA Issues Alert on Medical Devices Lacking Conformity Markings in the UK

The UK's Medicines and Healthcare products Regulatory Agency (MHRA) has advised healthcare professionals to immediately stop using and supplying certain medical devices that do not have the appropriate conformity markings. Although no specific defects or safety signals have been identified, the lack of proper assessment means there is insufficient assurance that these products meet UK regulatory requirements for quality, safety, and sterility. Affected devices include those used for blood collection, infusion, surgical procedures, wound management, and skin preparation. Organizations are instructed to quarantine existing stock and use compliant alternatives.