SAN2401 - National adverse incident reporting and safety alert systems for medical devices, IVDs, estates, facilities, social care equipment and PPE
Information request and response for FOI Reference: FOI – 2023-000448
Information request and response for FOI Reference: FOI – 2023-000441
SIM2307 - Olympus high flow insufflation unit UHI-4 - over pressure
SIM2306 - Vernacare Clinisan Bodywash product recall due to contamination
Information request and response for FOI Reference: FOI – 2023-000446
SIM2305 - Restricting public access to information on ligatures, points of ligature and other means of self-harm
SAN2307 - Ceiling-to-floor overhead track & hoist systems: risk of collapse during use
SAN2306 - Medical devices intended for use in a sterile state: review of systems and procedures
MDSI2311 - Specific brands of carbomer eye gel: recall of AACARB eye gel, AACOMER eye gel and PUROPTICS eye gel – potential risk of infection
