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MHRA Device Safety Information – MDSI (SC) 2105

MDSI (SC) 2105 - Recall of BD Venflon Pro safety IV cannula

MDSI2107 - Recall of BD Venflon Pro safety and Venflon Pro IV cannula

British National Formulary (BNF) publications reflect current best practice as well as legal and professional guidelines.

NatPSA/2021/001/MHRA - Supply disruption of sterile infusion sets and connectors manufactured by Becton Dickinson (BD)

IM/2020/001 - BD Neoflon™ Cannula (Straight IV Cannula for paediatric/neonatal use)

MDSI2304 - BD BodyGuard MicroSets and residual ethylene oxide: devices may continue to be used to treat paediatric patients 5kg and above

Find out more about our digital education programme for staff working in transfusion.

Scottish Health Technical Memorandum 61 and Appendix 1: provides specification and design guidance on building components for health buildings.

IM/2021/001 - Supply disruption of sterile infusion sets and connectors manufactured by Becton Dickinson (BD)

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