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11 results found
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)
MHRA Device Safety Information (MDSI)
MHRA Device Safety Information (MDSI) MDSIs capture safety information from MHRA. The information is about safety concerns which do not meet MHRAs cri
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