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MHRA Device Safety Information – MDSI2109

MDSI2109 - Handpieces used in the phacoemulsification technique of cataract removal: need for careful cleaning (DSI/2021/009)

MDSI2108 - Medical devices sterilised by Steril Milano - potential for incomplete sterilisation

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

Find out about the legislation and regulations for medical devices and in-vitro diagnostic medical devices, and the Health Institution Exemption.

NatPSA/2021/005/MHRA - Philips ventilator, CPAP and BiPAP devices: Potential for patient harm due to inhalation of particles.

IM/2020/022 - Regulation of medical devices and in-vitro diagnostic medical devices

SAN2306 - Medical devices intended for use in a sterile state: review of systems and procedures

MDSI2403 - Counterfeits and unbranded copies of LifeVac anti-choking devices may fail to work correctly or worsen choking incidents if used.

MDSI2310 - SteriFeed Colostrum Collection device and risk of choking due to infant airway occlusion.

National Decontamination Guidance on Loan Medical Devices (Reusable): Roles & Responsibilities GUID 5002