Zimmer, Inc.
299 recalls on record · Latest: Dec 31, 2025
FDA Devices Moderate Feb 26, 2014
M/DN R-F IM NAIL 9MM DIA , 10 MM, 11 MM, 12 MM, 13 MM and 14 MM. Item codes starting with 0022400
FDA Devices Moderate Feb 26, 2014
INTERLOCKING IM SCREW 4.5 and INTERLOCKING IM SCREW LG Some items starting with codes 0022530
FDA Devices Moderate Feb 26, 2014
NEXGEN OSTEOTOMY CORT BON. Item codes starting with 0052500
FDA Devices Moderate Jan 22, 2014
Palacos¿ R+G Radioplaque Bone Cement 1 x 40 g Single (with Gentamicin), 40.8 g Methyl Acrylate Copolymer, 20 ml Methyl Methacrylate Monomer 0.5 g Gen…
FDA Devices Moderate Jan 8, 2014
NGK Stem Ext 24 x 245mm
FDA Devices Moderate Jan 8, 2014
DIST LAT FEM LOCK PLT, RT
FDA Devices Moderate Jan 8, 2014
Versys Build-Up Block The VerSys CRC Hip System is indicated for total hip arthroplasty in patients whose bone stock is of poor quality or inadequ…
FDA Devices Moderate Jan 8, 2014
CPT Hip System, Parts 00-8114-002-10 and 00-8011-004-00 Hip joint metal/polymer semi-constrained cemented prosthesis. The CPT Hip System is indic…
FDA Devices Moderate Jan 8, 2014
FEM COND BUTTRESS PLT, LT
FDA Devices Moderate Jan 8, 2014
TIB NAIL
FDA Devices Moderate Dec 18, 2013
NexGen¿ Complete Knee Solutions Stemmed Tibial Component Precoat NexGen Tibial Baseplates are part of the NexGen systems of semi-constrained, non-…
FDA Devices Moderate Dec 18, 2013
NexGen Complete Knee Solution Porous Patella Drill Guide-26mm dia./10mm thickness Non sterile, Rx Only Devices are used in total knee arthroplas…
FDA Devices Moderate Dec 18, 2013
Zimmer Trabecular Metal Total Ankle Tibial Base Component Sizes 1-6 Total ankle arthroplasty is intended to provide a patient with limited mobili…
FDA Devices Moderate Dec 18, 2013
NexGen Complete Knee Solution CR Articular Surface Provisional-Yellow 9mm Height Nonsterile Devices are used in total knee arthroplasty and indic…
FDA Devices Moderate Dec 18, 2013
NexGen Complete Knee Solution CR Articular Surface Provisional-Purple 9mm Height Nonsterile Devices are used in total knee arthroplasty and indi…
FDA Devices Moderate Dec 18, 2013
NexGen Complete Knee Solution Porous Patella Drill Guide-29mm dia./10mm thickness Non sterile, Rx Only Devices are used in total knee arthroplas…
FDA Devices Moderate Dec 18, 2013
Zimmer Trabecular Metal Total Ankle Talar Component Right Sizes 1-6 Total ankle arthroplasty is intended to provide a patient with limited mobilit…
FDA Devices Moderate Dec 18, 2013
NexGen Complete Knee Solution CR Articular Surface Provisional-Striped Green 9mm Height Nonsterile Devices are used in total knee arthroplasty an…
FDA Devices Moderate Nov 27, 2013
Trinica Anterior Lumbar Plate (ALP) system, part 07.01058.001. Non Sterile, Rx only. The Trinica Anterior Lumbar Plate System is a temporary supplem…
FDA Devices Moderate Nov 20, 2013
VerSys¿ Cemented Revision Calcar (CRC) Hip System Femoral Stems VerSys Heritage Hip System Revision Femoral Stems. Indicated for total hip arthro…
FDA Devices Moderate Nov 13, 2013
Ti-Magna Fx Washer Ti-Versa-FX¿II Femoral Fixation System S/C Plates The compression tube/plates of this trauma system are used with Ti-Versa-F…
FDA Devices Moderate Nov 6, 2013
Natural-Knee¿ Flex Femoral Component. Provides increased flexion capability.
FDA Devices Moderate Nov 6, 2013
CoCr Head (Not distributed in the United States) Used in total hip replacement.
FDA Devices Moderate Nov 6, 2013
NexGen CR-Flex Mobile Bearing Tibial Component 9 (Not distributed in the United States)
FDA Devices Moderate Nov 6, 2013
Metasul¿ Head. Intended for use either with or without bone cement in total hip arthroplasty.
FDA Devices Moderate Nov 6, 2013
Zimmer¿ Unicompartmental Knee Femoral Component. Indicated for patients with painful and/or disabling knee joint.
FDA Devices Moderate Nov 6, 2013
Multipolar¿ Bipolar Cup METAL SHELL 38 MM OD through 71 MM OD. Indicated in fracture dislocation of the hip.
FDA Devices Moderate Nov 6, 2013
NexGen¿ Femoral Component (CR-FLEX GSF POR FEM, C-L; CR-FLEX GSF POR FEM, C-R; CR-FLEX GSF POR FEM, C-L MINUS; CR-FLEX GSF POR FEM, C-R MINUS; CR-FLE…
FDA Devices Moderate Nov 6, 2013
Gender Solutions" Patello-Femoral Component
FDA Devices Moderate Nov 6, 2013
NexGen¿ Femoral Component (CR-FLEX GSF PRECOAT SZ C-L; CR-FLEX GSF PRECOAT SZ C-R ; CR-FLEX GSF PCT SZ C-L MINUS; CR-FLEX GSF PCT SZ C-R MINUS ;C…
FDA Devices Moderate Sep 4, 2013
VERSA-FX II FEMORAL FIXATION SYSTEM COMPRESSION TUBE/PLATE, standard and short - low profile, different hole/length combinations (4/86, 5/102 and 6/1…
FDA Devices Moderate Sep 4, 2013
Free Lock Femoral Hip Fixation System Compression Lag Screw . Several lengths (55 to 150 mm) and diameters (12.7 and 15. 8 mm). Item codes starting w…
FDA Devices Moderate Aug 28, 2013
90597003109 Articular Surface CR ART SURF 34/STR YEL 09MM, Rx, Sterile; 90597003110 Articular Surface CR ART SURF 34/STR YEL 10MM, Rx, Sterile; …
FDA Devices Moderate Aug 28, 2013
65595201201 Femur CR-FLEX POR HATCP FEM B-L Rx, Sterile; 65595201202 Femur CR-FLEX POR HATCP FEM…
FDA Devices Moderate Aug 28, 2013
00597002009 Articular Surface CR ART SURF 12/PURPLE 9, Rx, Sterile; 00597002010 Articular Surface CR ART SURF 12/PURPLE 10, Rx, Sterile; 005970…
FDA Devices Moderate Aug 28, 2013
00595601201 Femur CR-FLEX OPT FEM B-L Rx Sterile; 00595601202 Femur CR-FLEX OPT FEM B-R Rx Sterile; Used in total knee arthroplasty and ind…
FDA Devices Moderate Aug 28, 2013
90597004109 Articular Surface CR ART SURF AE56/STR GRN 09MM, Rx, Sterile; 90597004110 Articular Surface CR ART SURF AE56/STR GRN 10MM, Rx, Sterile…
FDA Devices Moderate Aug 28, 2013
90597002009 Articular Surface CR ART SURF 12/PURPLE 09MM, Rx, Sterile; 90597002010 Articular Surface CR ART SURF 12/PURPLE 10MM, Rx, Sterile; 9…
FDA Devices Moderate Aug 28, 2013
00597001303 Femur CR PRC FEM COMP SIZE CML Rx, Sterile; 00597001304 Femur CR PRC FEM COMP SIZE CMR Rx, Sterile; 00597001403 Femur CR PRC FE…
FDA Devices Moderate Aug 28, 2013
00597206126 Patella ALL POLY PAT COMP MICRO 26DIA, Rx, Sterile; 00597206129 Patella ALL POLY PAT COMP MICRO 29DIA, Rx, Sterile; 00597206132 Pa…
FDA Devices Moderate Aug 28, 2013
00597103110 Provisional CR ART SURF PROV 34/STR YEL 10, Rx, Sterile; 00597103112 Provisional CR ART SURF PROV 34/STR YEL 12, Rx, Sterile; 005…
FDA Devices Moderate Aug 28, 2013
00595204110 Articular Surface XLPE CR ART SURF 5-6/STRGRN 10, Rx, Sterile; 00595204112 Articular Surface XLPE CR ART SURF 5-6/STRGRN 12, Rx, Steri…
FDA Devices Moderate Aug 28, 2013
00595202010 Articular Surface XLPE CR ART SURF 1,2/PUR 10, Rx, Sterile; 00595202012 Articular Surface XLPE CR ART SURF 1,2/PUR 12, Rx, Sterile; …
FDA Devices Moderate Aug 28, 2013
00597003109 Articular Surface CR ART SURF 34/STRIPE YEL 9, Rx, Sterile; 00597003110 Articular Surface CR ART SURF 34/STRIPE YEL 10, Rx, Sterile; …
FDA Devices Moderate Aug 28, 2013
00597201101 Femur CR POROUS FEM COMP SIZE AML Rx, Sterile; 00597201102 Femur CR POROUS FEM COMP SIZE AMR Rx, Sterile; 00597201201 Femur CR POR…
FDA Devices Moderate Aug 28, 2013
00597001333 Femur CR PRC SURF HDN FEM CO-NID CML Rx, Sterile; 00597001334 Femur CR PRC SURF HDN FEM CO-NID CMR Rx, Sterile; 00597001433 Femur…
FDA Devices Moderate Aug 28, 2013
00595501201 Provisional CR-FLEX FEM PROV SZ B-L, Rx, Sterile; 00595501202 Provisional CR-FLEX FEM PROV SZ B-R, Rx, Sterile; Used in total kne…
FDA Devices Moderate Aug 28, 2013
00597201333 Femur CR POR SURF HDN FEM CO-NID CML, Rx, Sterile; 00597201334 Femur CR POR SURF HDN FEM CO-NID CMR, Rx, Sterile; 00597201433 Femur…
FDA Devices Moderate Aug 28, 2013
00597104110 Provisional CR ART SURF PROV 56/STR GRN 10, Rx, Sterile; 00597104112 Provisional CR ART SURF PROV 56/STR GRN 12, Rx, Sterile; 005…
FDA Devices Moderate Aug 28, 2013