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MHRA Device Safety Information – MDSI (SC) 2105

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

Find out how our authorised engineers can help with your decontamination needs.

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

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

Specialising in the measurement and interpretation of trace elements and vitamins in clinical samples. Find out more.

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

An explanation of the calculations and adjustment types used in the eSchedule.

Our annual review and accounts for 2021 to 2022 details NSS's achievements over the past year.

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