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MHRA Device Safety Information – MDSI2304
MDSI2304 - BD BodyGuard MicroSets and residual ethylene oxide: devices may continue to be used to treat paediatric patients 5kg and above
MHRA Device Safety Information – MDSI2305
MDSI2305 - Belzer UW Cold Storage Solution & MPS UW Machine Perfusion Solution manufactured by Carnamedica: Contamination (update to DSI/2023/002)
MHRA Device Safety Information – MDSI2301
MDSI2301 - EyeCee One preloaded and EyeCee One Crystal preloaded intraocular lenses (IOLs): stop using immediately and quarantine all preloaded lenses
MHRA Device Safety Information – MDSI2204
MDSI2204 - Haemodialysis & haemofiltration machine: Actions to take following pressure-related alarms to avoid unintentional alteration of alarm limit
MHRA Device Safety Information – MDSI2203
MDSI2203 - Paclitaxel drug-coated balloons or drug-eluting stents: updated position
MHRA Device Safety Information – MDSI2202
MDSI2202 - Surdial X Haemodialysis machine: potential for devices to remove excess fluid outside of machine specification
MHRA Device Safety Information – MDSI2201
MDSI2201 - Gemini Surgical UK: Stop using all lots and batches of vaginal speculums with smoke tube and gynaecological hysteroscopy sheaths
MHRA Device Safety Information – MDSI2110
MDSI2110 - Baihe Rheovalves disposable needle-free valves: stop using specific lots due to risk of breakage in patient
MHRA Device Safety Information – MDSI2109
MDSI2109 - Handpieces used in the phacoemulsification technique of cataract removal: need for careful cleaning (DSI/2021/009)
MHRA Device Safety Information – MDSI2108
MDSI2108 - Medical devices sterilised by Steril Milano - potential for incomplete sterilisation