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FOI – 000148 STOMA Cap Meetings
Information request and response for FOI Reference: FOI – 000148
FOI – 2022-000077 Marketing And Communications team
Information request and response for FOI Reference: FOI – 2022-000077
MHRA Medical Device Safety Information – MDSI2310
MDSI2310 - SteriFeed Colostrum Collection device and risk of choking due to infant airway occlusion.
Safety Action Notice – SAN2205
SAN2205 – Recall of hygiene products associated with Pseudomonas aeruginosa infection.
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DSI/2025/001- Suzhou Surgicare disposable Hysteroscopy Sheath – recall due to withdrawn CE certificate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