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When to report an incident to us

Information about when you should report an adverse incident.

Scottish Health Technical Memorandum 01-01 Parts A, B, C, D, E and F, GUID 5017 and 5019: decontamination of medical devices processed through a CDU.

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

Additional learning resources include IRIC spotlight session recordings and medical device e-learning modules.

SIM2210 - IPEM guidance for health institutions on in-house manufacture and use, including software (2nd Ed.)

MDSI (SC) 2104 - Total parenteral (TPN) and enteral nutrition bags manufactured by Diffuplast: Sterilisation issue

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.