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MHRA Device Safety Information – MDSI2303
MDSI2303 - Zimmer Biomet NexGen Knee replacement: affected patients should be offered additional follow up.
Safety Action Notice – SAN2205(U2)
SAN2205(U2) - Recall of hygiene products associated with Pseudomonas aeruginosa infection (Update)
Safety action notices
View the latest safety action notices issued by IRIC.