Zimmer recalls
Zimmer appears in 545 official U.S. recall notices indexed by RecallRadar.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
- 90595203117 Articular Surface XLPE CR ART SURF AE34/STYEL 17, Rx, Sterile
FDA Device · Class II · 2013-08-28 · Zimmer - 00595203110 Articular Surface XLPE CR ART SURF 3,4/SYEL 10, Rx, Sterile
FDA Device · Class II · 2013-08-28 · Zimmer - 00597603110 Articular Surface AC ART SURF 34/STRIPED YEL 10, Rx, Sterile
FDA Device · Class II · 2013-08-28 · Zimmer - 65595201201 Femur CR-FLEX POR HATCP FEM B-L Rx, Sterile
FDA Device · Class II · 2013-08-28 · Zimmer - 00597201333 Femur CR POR SURF HDN FEM CO-NID CML, Rx, Sterile
FDA Device · Class II · 2013-08-28 · Zimmer - 00597001303 Femur CR PRC FEM COMP SIZE CML Rx, Sterile
FDA Device · Class II · 2013-08-28 · Zimmer - 90595204117 Articular Surface XLPE CR ART SURF AE56/STGRN 17, Rx, Sterile
FDA Device · Class II · 2013-08-28 · Zimmer - 00597106126 Provisional MIC POROUS PAT PROV 26MMX10MM, Rx, Sterile
FDA Device · Class II · 2013-08-28 · Zimmer - 00587806126 Patella MICRO POROUS PAT 26MM X 10MM, Rx, Sterile
FDA Device · Class II · 2013-08-28 · Zimmer - 00597204109 Articular Surface CR ART SURF 56/STRIPE GRN 9, Rx, Sterile
FDA Device · Class II · 2013-08-28 · Zimmer - 00595601201 Femur CR-FLEX OPT FEM B-L Rx Sterile
FDA Device · Class II · 2013-08-28 · Zimmer - 65597201101 Femur CR POR FEM HATCP SIZE AML Rx, Sterile
FDA Device · Class II · 2013-08-28 · Zimmer - 90597004109 Articular Surface CR ART SURF AE56/STR GRN 09MM, Rx, Sterile
FDA Device · Class II · 2013-08-28 · Zimmer - 90597002009 Articular Surface CR ART SURF 12/PURPLE 09MM, Rx, Sterile
FDA Device · Class II · 2013-08-28 · Zimmer - 00597503110 Provisional AC ARTSURF PROV 34/STRIPE YEL10, Rx, Sterile
FDA Device · Class II · 2013-08-28 · Zimmer - 00595001201 Femur CR-FLEX PCT FEM B-L Rx, Sterile
FDA Device · Class II · 2013-08-28 · Zimmer - 00597004109 Articular Surface CR ART SURF 56/STRIPE GREEN 9, Rx, Sterile
FDA Device · Class II · 2013-08-28 · Zimmer - 90597003109 Articular Surface CR ART SURF 34/STR YEL 09MM, Rx, Sterile
FDA Device · Class II · 2013-08-28 · Zimmer - 00597203109 Articular Surface CR ART SURF 34/STRIPE YEL 09, Rx, Sterile
FDA Device · Class II · 2013-08-28 · Zimmer - 65597201333 Femur CR POR FEM SURF HDN HATCP CML, Rx, Sterile
FDA Device · Class II · 2013-08-28 · Zimmer - 00598706201 Provisional CRA FEM PROV/CUT GDE SZ BML, Rx, Sterile
FDA Device · Class II · 2013-08-28 · Zimmer - 00597001333 Femur CR PRC SURF HDN FEM CO-NID CML Rx, Sterile
FDA Device · Class II · 2013-08-28 · Zimmer - 00597202009 Articular Surface CR ART SURF 12/PURPLE 09, Rx, Sterile
FDA Device · Class II · 2013-08-28 · Zimmer - 00597101101 Provisional CR PROV FRM COMP SIZE AML, Rx, Sterile
FDA Device · Class II · 2013-08-28 · Zimmer - REF 00-4309-071-40 Trabecular Metal Reverse Shoulder System Instrumentation, Glenosphere Helmet, 40 mm Diameter Nonsterile, Qty -1 Instrume…
FDA Device · Class II · 2013-08-21 · Zimmer - REF 00-4309-071-36 Trabecular Metal Reverse Shoulder System Instrumentation, Glenosphere Helmet, 36 mm Diameter Nonsterile, Qty -1 Instrume…
FDA Device · Class II · 2013-08-21 · Zimmer - Bigliani/Flatow¿ The Complete Shoulder Solution, Humeral Stem Provisional 12mm x 170mm This reusable trial device is used in orthopaedic jo…
FDA Device · Class II · 2013-07-17 · Zimmer - Bigliani/Flatow¿ The Complete Solution Fukuda Retractors Small Nonsterile 00-4305-019-30
FDA Device · Class II · 2013-07-10 · Zimmer - Bigliani/Flatow¿ The Complete Solution Fukuda Retractors Large Nonsterile 4305-19-40
FDA Device · Class II · 2013-07-10 · Zimmer - Zimmer Patient Helper Bed Frame Adapter Assembly The bed frame adapter assembly is intended to be used by qualified medical professionals t…
FDA Device · Class II · 2013-06-26 · Zimmer - NEXGEN Complete Knee Solution Monoblock Tibial Drill with stop 10.7 mm
FDA Device · Class II · 2013-06-05 · Zimmer - Zimmer NexPosure, retractor portals of the NexPosure MIS Access System, Part Numbers or REF numbers: N1830R80-100, N1830R80-090¿, N1830R80-…
FDA Device · Class II · 2013-04-10 · Zimmer - Trilogy Acetabular Shells with Holes
FDA Device · Class II · 2013-02-13 · Zimmer - Trilogy F/M Acetabular Shell with Uni-Hole
FDA Device · Class II · 2013-02-13 · Zimmer - Trilogy Acetabular Shell Spiked
FDA Device · Class II · 2013-02-13 · Zimmer - Trilogy Acetabular AB Shells with Cluster Holes
FDA Device · Class II · 2013-02-13 · Zimmer - Trilogy F/M Acetabular Shell without holes
FDA Device · Class II · 2013-02-13 · Zimmer - Trilogy Acetabular Shell with Cluster Holes
FDA Device · Class II · 2013-02-13 · Zimmer - Trilogy F/M Acetabular Shell without holes SOLID HA. Several ODs: 38MM, 40MM, 42MM, 44MM, 46MM, 48MM, 50MM, 52MM, 54MM, 56MM, 58MM, 60MM, 6…
FDA Device · Class II · 2013-02-13 · Zimmer - Trilogy Acetabular AB Shells with Holes
FDA Device · Class II · 2013-02-13 · Zimmer - The TM Ardis Interbody System Inserter Stainless Steel, Rubber, Silicone Non Sterile Rx only
FDA Device · Class II · 2013-01-16 · Zimmer - Zimmer Spine Ardis Inserter, Rx, non-sterile
FDA Device · Class I · 2013-01-02 · Zimmer - Persona, The Personalized Knee System,Tibial Drill, Cemented, 15.7 mm Diameter, Nonsterile This device is indicated for patients with sever…
FDA Device · Class II · 2012-12-26 · Zimmer - Persona The Personalized Knee System, Natural Tibia, Cemented, 5 Degree Stemmed Tivanium Sterile TIBIA SIZE F, LEFT TIBIA SIZE F RIGHT This…
FDA Device · Class II · 2012-12-26 · Zimmer - Persona, The Personalized Knee System, Tibial Sizing Plate, Cemented, Nonsterile, Size F Left
FDA Device · Class II · 2012-12-26 · Zimmer - Persona, The Personalized Knee System, Tibial Sizing Plate, Cemented, Nonsterile, Size D Left
FDA Device · Class II · 2012-12-26 · Zimmer - Persona, The Personalized Knee System, Tibial Sizing Plate, Cemented, Nonsterile, Size C Left
FDA Device · Class II · 2012-12-26 · Zimmer - Persona, The Personalized Knee System, Tibial Drill Guide, Cemented, 15.7 mm Diameter, Nonsterile, Nonsterile This drill guide is used with…
FDA Device · Class II · 2012-12-26 · Zimmer - Persona The Personalized Knee System, Natural Tibia, Cemented, 5 Degree Stemmed Tivanium Sterile This device is indicated for patients with…
FDA Device · Class II · 2012-12-26 · Zimmer - Persona, The Personalized Knee System, Tibial Broach, Cemented, Size G-H, Nonsterile, This device is used with the Persona Knee System for…
FDA Device · Class II · 2012-12-26 · Zimmer