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MHRA Medical Device Safety Information – MDSI2309
MDSI2309 - BioIntegral Surgical Inc. No-React® cardiovascular bioprosthesis implantables: discontinuation of CE marking and manufacture
Device Safety Information – DSI/2025/001
DSI/2025/001- Suzhou Surgicare disposable Hysteroscopy Sheath – recall due to withdrawn CE certificate
Specialist services UK
Learn about how the NHS connects across borders to provide highly specialist care for patients in Scotland.
MHRA Device Safety Information – MDSI2306
MDSI2306 - NuVasive Specialized Orthopedics (NSO) PRECICE Titanium Systems: UK Suspension Lifted
FOI – 2022-000077 Marketing And Communications team
Information request and response for FOI Reference: FOI – 2022-000077
Safety Information Message – SIM2501(U)
SIM2501(U) - Product Safety Report: MK Electric MK Essentials Electrical Three Pin Sockets with Switches: risk of burns
MHRA Medical Device Safety Information – MDSI2311U
MDSI2311U - Specific brands of carbomer eye gel: recall of AACARB eye gel, AACOMER eye gel and PUROPTICS eye gel: potential risk of infection - UPDATE
Infected blood interim compensation payment announcement update
UK Government Announcement
FOI – 000172 Expertise of members in UK IPC Cell
Information request and response under the Freedom of Information (Scotland) Act 2002
First NHSScotland patients in a generation receive lifesaving UK plasma
The first NHSScotland patients in a generation have started to receive life-saving plasma derived medicines made from the blood of UK donors.