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FOI – 2022-000077 Marketing And Communications team

Information request and response for FOI Reference: FOI – 2022-000077

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DSI/2025/001- Suzhou Surgicare disposable Hysteroscopy Sheath – recall due to withdrawn CE certificate

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MHRA Device Safety Information – MDSI2306

MDSI2306 - NuVasive Specialized Orthopedics (NSO) PRECICE Titanium Systems: UK Suspension Lifted

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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

Web and channel services

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