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MHRA Device Safety Information – MDSI (SC) 2105

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

MDSI (SC) 2106 - Investigation update: CE mark suspended for all MAGEC systems manufactured by NuVasive Specialized Orthopedics, Inc.

Learn more about the GMDN – a medical device sorting machine.

MDSI (SC) 2103 - Dexcom G6 Sensor: untested barrier methods to reduce skin reactions.

MDSI (SC) 2101 - Paclitaxel drug-coated balloons (DCBs) or drug-eluting stents (DESs)

MDSI (SC) 2102 - Medoject sterile hypodermic and blunt fill needles manufactured by Chirana T. Injecta – discontinue use

(Archived) Scottish Health Facilities Note 03-03: Mobile Communication Devices

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IM/2021/005 - Changes to IRIC safety alerts

SAN2305 - SteriFeed Colostrum Collection device and risk of choking due to infant airway occlusion: supplementary advice