An MDA may come about as a result investigation by any of the UK administrations where the manufacturer can not demonstrate they have taken appropriate action. Alternatively they can result through other information received by the MHRA from Competent Authorities around the world.
Medical Device Alerts are distributed to the HSC Board, HSC Trusts, and Agencies for direct action and for onward transmission were appropriate in accordance with local procedures. NIAIC arranges for the distribution to Primary Care Professionals.
Anyone accessing this information must bear in mind that this information is directed at health and social care professionals and has been prepared taking into account the specialist knowledge of these intended recipients. Members of the public should contact their GP, health advisor or NIAIC if the content of a notice causes personal concern.
Each alert is sent to HPSS organisations where action is required to be taken. Any member of the public requiring information on a particular notice is advised to contact their General Practitioner or NIAIC directly.