Biomet recalls
Biomet appears in 279 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.
- Comprehensive Shoulder System, 4 mm, 122 mm long, Primary Shoulder Stem, Ti-6Al-4V, Standard Length Porous Plasma
FDA Device · Class III · 2015-06-17 · Biomet - Biomet Cobalt-Chrome Femoral Components, 32MM MOD HEAD COCR -6MM NECK
FDA Device · Class III · 2015-06-17 · Biomet - Unilateral external fixation ankle clamp Product Usage: Unilateral external fixation for use treatment of bone conditions amenable to treat…
FDA Device · Class II · 2015-06-17 · Biomet - LOW PROFILE NON-LOCK SCREW
FDA Device · Class II · 2015-04-22 · Biomet - ToggleLoc
FDA Device · Class II · 2015-04-08 · Biomet - Ziploop Button Product Usage: The Ziploop Button is a non-resorbable system intended to aid in ACL reconstructive procedure due to injury o…
FDA Device · Class II · 2015-04-08 · Biomet - Comprehensive Reverse Shoulder Glenosphere Mini Baseplate 25mm with Taper Adaptor, Part Number: 010000589 Lot: 527400
FDA Device · Class II · 2015-03-04 · Biomet - Mallory Head 4 Finned Acetabular Shell 50 mm, PN 13-104150, hip prosthesis component (Ringloc)
FDA Device · Class II · 2015-02-25 · Biomet - Ringloc+ Acetabular Shell Finned 52 mm, PN 16-104152, hip prosthesis component
FDA Device · Class II · 2015-02-25 · Biomet - Device Brand Name: Sirius Polish Cemented Stem 34B Device Classification Name: prosthesis, hip, semi-constrained, metal/polymer, cemented D…
FDA Device · Class II · 2014-12-24 · Biomet - Sirius Polish Cemented Stem 38C Catalog Number: 51-199335 Lot Number Identification: 141680, 180920 The Biomet's Sirius Femoral Hip Stem is…
FDA Device · Class II · 2014-12-24 · Biomet - Discovery Elbow Humeral Trial Product Usage: Biomet manufactures a variety of elbow joint replacement prostheses intended for primary and r…
FDA Device · Class II · 2014-10-22 · Biomet - Compress Face Reamer Product Usage: Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement, tumor res…
FDA Device · Class II · 2014-10-15 · Biomet - Black Mamba Suture Passer
FDA Device · Class II · 2014-10-15 · Biomet - Mamba Disposable Nitinol Needle
FDA Device · Class II · 2014-10-15 · Biomet - Green Mamba Suture Passer
FDA Device · Class II · 2014-10-15 · Biomet - Vanguard 360 Femoral Boss Reamer, Label: REF 32-488474 VANGUARD 360 1NSTRUMENT FEMORAL BOSS REAMER NON-STERILE, BIOMET ORTHOPEDICS 56 EAST…
FDA Device · Class II · 2014-08-27 · Biomet - Device Brand Name: Distal Radius Fracture Repair System Device Classification Name: Plate, Fixation, Bone Device Common Name: Drill Guide D…
FDA Device · Class II · 2014-08-20 · Biomet - DISCOVERY ELBOW prosthesis, 4 MM X 100 MM RIGHT HUMERAL FLANGED I BOND COAT Tl 6AL 4V ALLOY. Elbow joint replacement prostheses are intende…
FDA Device · Class II · 2014-07-02 · Biomet - EZPass Passer, Sterile single use arthroscopic instrument utilized in conjunction with a nitinol wire to aid in passing suture through soft…
FDA Device · Class II · 2014-06-25 · Biomet - G7 Acetabular System Positioning Guide Post, orthopedic surgical instrument for hip prosthesis
FDA Device · Class II · 2014-06-25 · Biomet - G7 Acetabular System Positioning Guide Rod, orthopedic surgical instrument for hip prosthesis PN 110003458
FDA Device · Class II · 2014-06-25 · Biomet - EZPass Nylon Monofilament Single Pack, Part number 110007379, Orthopedic Manual Surgical Instrument Sterile, single use arthroscopic instru…
FDA Device · Class II · 2014-06-25 · Biomet - EZPass Suture Retriever, Nitinol, Single Pack, Part number 10007380
FDA Device · Class II · 2014-06-25 · Biomet - ExploR 7x26mm Modular Radial Stem, Catalog number 11-210062
FDA Device · Class II · 2014-05-21 · Biomet - Part 475620 Intramedullary Bone Saw CAM Assembly Size 12mm, A unique and exclusive clinical instrument used to correct leg length, or rotat…
FDA Device · Class II · 2014-03-26 · Biomet - Part 475625, Intramedullary Bone Saw, Cam Assembly Size 13 mm, The Biomet Intramedullary Bone Saw is a unique and exclusive clinical instru…
FDA Device · Class II · 2014-03-26 · Biomet - Part 475630, Intramedullary Bone Saw, Cam Assembly Size 14 mm, The Biomet Intramedullary Bone Saw is a unique and exclusive clinical instru…
FDA Device · Class II · 2014-03-26 · Biomet - Locking Cortical Screw 3.5mmX38mm REF 8161-35-038
FDA Device · Class II · 2014-01-22 · Biomet - G7 Acetabular Screw 6.5mmx35mm Part Number: 010001000
FDA Device · Class II · 2014-01-01 · Biomet - outer box: Ref 906768, CurvTek Eye Needle 22 MM X-large Stainless Steel, Single Use Gamma Sterilized, Rx inner incorrect label: CurvTek 7 M…
FDA Device · Class II · 2013-12-25 · Biomet - REF 200068 Security (TM) Enclosed Carpal Tunnel System Blade ( Single) ABS /Stainless Steel Sterile Device, Single Use Only
FDA Device · Class II · 2013-12-04 · Biomet - Juggerknotless Drill Bit, REF 110003173, Sterile, Single Use Product Usage: The Juggerknotless Soft Anchors are indicated for soft tissue r…
FDA Device · Class II · 2013-11-27 · Biomet - REF 154223 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size D5 ARCOM UHMWPE / CO-CR-MO Alloy Only for use in Lateral compartme…
FDA Device · Class II · 2013-07-17 · Biomet - REF 154232 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size E7 ARCOM UHMWPE / CO-CR-MO Alloy Only for use in Lateral compartme…
FDA Device · Class II · 2013-07-17 · Biomet - REF 154235Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size F3 ARCOM UHMWPE / CO-CR-MO Alloy Only for use in Lateral compartmen…
FDA Device · Class II · 2013-07-17 · Biomet - REF 154200 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size A3 ARCOM UHMWPE / CO-CR-MO Alloy Only for use in Lateral compartme…
FDA Device · Class II · 2013-07-17 · Biomet - REF 154221 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size D3 ARCOM UHMWPE / CO-CR-MO Alloy Only for use in Lateral compartme…
FDA Device · Class II · 2013-07-17 · Biomet - REF 154236 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size F4 ARCOM UHMWPE / CO-CR-MO Alloy Only for use in Lateral compartme…
FDA Device · Class II · 2013-07-17 · Biomet - REF 154215 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size C4 ARCOM UHMWPE / CO-CR-MO Alloy Only for use in Lateral compartme…
FDA Device · Class II · 2013-07-17 · Biomet - REF 154208 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size B4 ARCOM UHMWPE / CO-CR-MO Alloy Only for use in Lateral compartme…
FDA Device · Class II · 2013-07-17 · Biomet - REF 154228 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size E3 ARCOM UHMWPE / CO-CR-MO Alloy Only for use in Lateral compartme…
FDA Device · Class II · 2013-07-17 · Biomet - REF 154201 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size A4 ARCOM UHMWPE / CO-CR-MO Alloy Only for use in Lateral compartme…
FDA Device · Class II · 2013-07-17 · Biomet - REF 154214 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size C3 ARCOM UHMWPE / CO-CR-MO Alloy Only for use in Lateral compartme…
FDA Device · Class II · 2013-07-17 · Biomet - REF 154224 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size D6 ARCOM UHMWPE / CO-CR-MO Alloy Only for use in Lateral compartme…
FDA Device · Class II · 2013-07-17 · Biomet - REF 154210 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size 6ARCOM UHMWPE / CO-CR-MO Alloy Only for use in Lateral compartment…
FDA Device · Class II · 2013-07-17 · Biomet - REF 154225Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size D7 ARCOM UHMWPE / CO-CR-MO Alloy Only for use in Lateral compartmen…
FDA Device · Class II · 2013-07-17 · Biomet - REF 154202 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size A5 ARCOM UHMWPE / CO-CR-MO Alloy Only for use in Lateral compartme…
FDA Device · Class II · 2013-07-17 · Biomet - REF 154207 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size B3 ARCOM UHMWPE / CO-CR-MO Alloy Only for use in Lateral compartme…
FDA Device · Class II · 2013-07-17 · Biomet - REF 154229 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size E4 ARCOM UHMWPE / CO-CR-MO Alloy Only for use in Lateral compartme…
FDA Device · Class II · 2013-07-17 · Biomet