Radiologists use and manage a very wide range of medicines and medical devices and this page has been specifically adapted to their needs. It includes guidance, safety alerts and links to educational material to assist radiologists in the safe use and management of medicines and medical devices.
Latest news and hot topics
21 Nov 2013 | Medical Device Alert: Perfusor Space infusion pump manufactured by B Braun (MDA/2013/080)
This Medical Device Alert has been issued as there is a risk of interruption of therapy when changing syringe.
04 Nov 2013 | Medical Device Alert: Infusion pumps - Plum A+ and A+3 family of infusers, Gemstar infuser and Lifecare PCA infuser manufactured by Hospira (MDA/2013/078)
This Medical Device Alert has been issued as the CE marking for these pumps has been withdrawn. Hospira will not be able to supply any new pumps. However, they can continue to supply consumables for pumps already in use.
30 Oct 2013 | Medical Device Alert: Receptal suction canisters and liners manufactured by Hospira (formerly manufactured by Abbott) (MDA/2013/077)
This Medical Device Alert has been issued as there is potential for failure or loss of suction if a canister and liner of different sizes are used in combination when using receptal suction canisters and liners manufactured by Hospira.
16 Oct 2013 | Medical Device Alert: Vacutainer® multiple sample Luer adaptor for blood sample collection manufactured by Becton, Dickinson and Company (BD) (MDA/2013/075)
This Medical Device Alert has been issued increased risk to users of exposure to blood, and a risk of under filling blood collection tubes which could lead to unexpected results in some laboratory tests, when using Vacutainer® multiple sample Luer adaptors manufactured by Becton, Dickinson and Company (BD).
11 Oct 2013 | Tell us what you think
The MHRA is seeking feedback on the information it communicates to the health and social care sector about risks relating to medicines and medical devices.
Drug Safety Update (DSU)
Interactive education modules
Annually many patients and staff are injured needlessly by medical devices that are either used incorrectly or badly maintained. These injuries are often due to user error or poor systems of work, not the device function or design. In these education packages we have tried to give a generic overview of some of the devices that have been reported to us as problematic.
We have produced a series of educational packages that are simple to use, informative and should take no more than thirty minutes to work through. They have all been developed by MHRA staff, some in conjunction with and endorsement by royal colleges and some attract CPD points. They provide valuable dos and don’ts when using and operating medical devices.
Links to further information
|British Institute of Radiology (BIR) (external link)|
|British Society of Gastro-intestinal and Abdominal Radiologists (external link)|
|British Society of Interventional Radiology (external link)|
|British Society of Neuroradiologists (external link)|
|British Society of Skeletal Radiology (external link)|
|National Institute for Health and Clinical Excellence (NICE) (external link)|
|NHS National Library for Health (external link)|
|NHS Purchasing and Supply Agency - Centre for Evidence-based Purchasing (external link)|
|Royal College of Radiologists (external link)|
|Society of Radiographers (external link)|
|MHRA information and guidance|
|Mobile communications interference|
Updates to your inbox
Reporting of adverse incidents or adverse drug reactions
Any actual, suspected, potential or avoided adverse event should be reported. Further examples of cases which should be reported are available in the sections below. If in doubt, please report. You can help us by reporting adverse incidents. These reports enable us to identify medical devices and medicines that are of concern and allow us to take appropriate action.
What should I report if I suspect a medicine is associated with an adverse reaction?
Please complete a Yellow Card to report suspected adverse reactions to prescription medicines, over-the-counter medicines, or herbal remedies. For further information, please see www.yellowcard.gov.uk (external link).
Please clarify what a medical device is and what I should report?
Please see our section on reporting safety problems.
Medical Device Alerts (MDAs)
Report counterfeit medicines and devices
If you have been offered what you suspect to be counterfeit products, or have seen them for sale or have bought them we would like you to tell us.
If you have any concerns or information that may assist us in tracking down those responsible for counterfeit medicines and devices you can:
- email the Enforcement Group at email@example.com
- ring our 24 hour dedicated hotline on 020 3080 6701
- write to us at Counterfeits, The Intelligence Unit, MHRA, 151 Buckingham Palace Road, Victoria, London, SW1W 9SZ.
Guidance and publications
One Liners is a short, news sheet for healthcare professionals which highlight problems with medical devices. It is a review of user issues that have been brought to our attention and are generally reports of continuing misuse of simple medical equipment.
All medical devices can fail but an increasing number of incidents reported arise out of user problems or poor practices. The aim of the One Liner is to briefly detail some of these problems in an attempt to make users more aware of what can go wrong - it is all too easy to take equipment for granted.