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Name Date Date initiated Country Source
Field Safety Notices about Mpower Switzerland SATP
Field Safety Notices about PowerPro Model, S/N: see letter Switzerland SATP
Field Safety Notices about PowerProMax Model, S/N: see letter Switzerland SATP
Field Safety Notices about Offset Cup Impactor Switzerland SATP
Field Safety Notices about Standard Offset Cup Impactor Switzerland SATP
Field Safety Notices about PROFEMUR Neck Var/Val Long CoCr Switzerland SATP
Field Safety Notices about Synex-II Central Body Switzerland SATP
Field Safety Notices about powerpro, powerpromax and mpower cordless devices 2009-10-12 Poland ORMPMDBP
Field Safety Notices about offset cup impactor (POM-C) 2017-04-28 Poland ORMPMDBP
Field Safety Notices about postoperative femoral neck fractures profemur neck var / val 8dg long cocr 2015-09-07 Poland ORMPMDBP
Field Safety Notices about brachial arm of the complete inverted shoulder system , manufactured before september 2011. 2017-03-02 Poland ORMPMDBP
Recall of OPTIVAC VACUUM MIXING SYSTEM FOR BONE CEMENT 2005-02-25 Canada HC
Recall of TEFLON TUBE - STERILE 2013-11-04 Canada HC
Recall of ADJUSTABLE DRILL STOPS 2012-04-16 Canada HC
Recall of STERNALOCK BLU IMPLANT TRAY 2011-12-06 Canada HC
Recall of SYNEX II SYSTEM - CENTRAL BODY 2009-09-23 Canada HC
Recall of ACTIFUSE ABX 2015-08-19 Canada HC
Recall of OTISMED SHAPEMATCH CUTTING GUIDE 2013-04-15 Canada HC
Recall of VANGUARD TOTAL KNEE SYSTEM - DCM - PS PLUS TIBIAL BEARINGS 2017-02-21 Canada HC
Recall of NEXGEN COMPLETE KNEE SOLUTION STEMMED NON-AUGMENT TIBIAL COMP (CR/PS)OPTION 2012-10-01 Canada HC
Recall of ADVANCED CEMENT MIXING BOWL EMPTY CEMENT CARTRIDGE NOZZLE AND PRESSURIZER 2017-11-22 Canada HC
Recall of PT HYBRID GLENOID POST 2012-12-07 Canada HC
Recall of Device Recall BHR Acetabular Cup W/ Impactor 2007-03-13 United States USFDA
Recall of Device Recall BHR Acetabular Cup W/ Impactor 2007-03-13 United States USFDA
Recall of Device Recall BHR Acetabular Cup W/ Impactor 2007-03-13 United States USFDA