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Early Re-examination Guidance
The Early Re-examination Guidance
MHRA Device Safety Information – MDSI (SC) 2105
MDSI (SC) 2105 - Recall of BD Venflon Pro safety IV cannula
MHRA Device Safety Information – MDSI2107
MDSI2107 - Recall of BD Venflon Pro safety and Venflon Pro IV cannula
National Patient Safety Alert – NatPSA/2021/001/MHRA
NatPSA/2021/001/MHRA - Supply disruption of sterile infusion sets and connectors manufactured by Becton Dickinson (BD)
Information Message - IM/2020/001
IM/2020/001 - BD Neoflon™ Cannula (Straight IV Cannula for paediatric/neonatal use)
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
Information Message - IM/2021/001
IM/2021/001 - Supply disruption of sterile infusion sets and connectors manufactured by Becton Dickinson (BD)
NSS Statement of Public Task
NSS Statement of Public Task
MHRA Device Safety Information – MDSI2204
MDSI2204 - Haemodialysis & haemofiltration machine: Actions to take following pressure-related alarms to avoid unintentional alteration of alarm limit
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