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MHRA Medical Device Safety Information – MDSI2407
MDSI2407 - Zimmer CPT Hip System Femoral Stem 12/14 Neck Taper: increased risk of postoperative periprosthetic femoral fracture
MHRA Medical Device Safety Information – MDSI2311U
MDSI2311U - Specific brands of carbomer eye gel: recall of AACARB eye gel, AACOMER eye gel and PUROPTICS eye gel: potential risk of infection - UPDATE
MHRA Medical Device Safety Information – MDSI2403
MDSI2403 - Counterfeits and unbranded copies of LifeVac anti-choking devices may fail to work correctly or worsen choking incidents if used.
MHRA Medical Device Safety Information – MDSI2405
MDSI2405 - Symbios ORIGIN® Posterior Stabilised Patient-Matched Total Knee Replacement Device: Risk of Early Revision
MHRA Medical Device Safety Information – MDSI2404
MDSI2404 - Legency Remedies 0.9% Sodium Chloride Solutions for Irrigation, Inhalation, and Eyewash: risk of microbiological contamination
MHRA Medical Device Safety Information – MDSI2401
MDSI2401 - Paclitaxel coated devices (PCD) used in the treatment of peripheral arterial disease: update to previous MHRA guidance on use.
MHRA Medical Device Safety Information – MDSI2311
MDSI2311 - Specific brands of carbomer eye gel: recall of AACARB eye gel, AACOMER eye gel and PUROPTICS eye gel – potential risk of infection
MHRA Medical Device Safety Information – MDSI2309
MDSI2309 - BioIntegral Surgical Inc. No-React® cardiovascular bioprosthesis implantables: discontinuation of CE marking and manufacture
MHRA Medical Device Safety Information – MDSI2310
MDSI2310 - SteriFeed Colostrum Collection device and risk of choking due to infant airway occlusion.