Biomet recalls
Biomet appears in 279 official U.S. recall notices indexed by RecallRadar, most recently on 2026-08-12.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
- Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475625 Product Description: Intramedullary Bone Saw Blade Assembly 13mm
FDA Device · Class II · 2026-08-12 · Biomet - Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475620 Product Description: Intramedullary Bone Saw Blade Assembly 12mm
FDA Device · Class II · 2026-08-12 · Biomet - Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475640 Product Description: Intramedullary Bone Saw Blade Assembly 16mm
FDA Device · Class II · 2026-08-12 · Biomet - Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475635 Product Description: Intramedullary Bone Saw Blade Assembly 15mm
FDA Device · Class II · 2026-08-12 · Biomet - Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475630 Product Description: Intramedullary Bone Saw Blade Assembly 14mm
FDA Device · Class II · 2026-08-12 · Biomet - BIOMET ZipTight, Acute AC Joint Implant, Single Ziploop , Model/Catalog Number: 904834
FDA Device · Class II · 2025-10-29 · Biomet - Juggerknot Mini Soft Anchors, Model/Catalog Number: 912080
FDA Device · Class II · 2025-10-01 · Biomet - JuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 110027357
FDA Device · Class II · 2024-11-27 · Biomet - RingLoc Bi-Polar Hip System Acetabular Cup, 41 mm Outer Diameter - Used in hip hemi-arthroplasty Item Number: 11-165206
FDA Device · Class II · 2024-07-03 · Biomet - Vanguard Knee System AS Tibial Bearing / DCM ArCom, 12 MM X 75 MM
FDA Device · Class II · 2024-05-01 · Biomet - Biolox Ceramic Option Head Zimmer 12/14 40mm -3, Item Number 00-8777-040-01
FDA Device · Class II · 2023-12-27 · Biomet - Biolox Ceramic Option Head Zimmer 12/14 40mm +0, Item Number 00-8777-040-02
FDA Device · Class II · 2023-12-27 · Biomet - Compress Device Segmental Anchor Plug, 18 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replaceme…
FDA Device · Class II · 2023-11-29 · Biomet - Compress Device Short Anchor Plug, 12 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement
FDA Device · Class II · 2023-11-29 · Biomet - Compress Device Segmental Anchor Plug, 20 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replaceme…
FDA Device · Class II · 2023-11-29 · Biomet - Compress Device Short Anchor Plug, 10 MM-Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement Item…
FDA Device · Class II · 2023-11-29 · Biomet - Compress Device Segmental Anchor Plug, 22 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replaceme…
FDA Device · Class II · 2023-11-29 · Biomet - Compress Device Segmental Anchor Plug, 16 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replaceme…
FDA Device · Class II · 2023-11-29 · Biomet - Compress Device Short Anchor Plug, 14 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement
FDA Device · Class II · 2023-11-29 · Biomet - Compress Device Segmental Anchor Plug, 12 MM -For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacem…
FDA Device · Class II · 2023-11-29 · Biomet - Compress Device Short Anchor Plug, 20 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement
FDA Device · Class II · 2023-11-29 · Biomet - Compress Device Segmental Anchor Plug, 24 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replaceme…
FDA Device · Class II · 2023-11-29 · Biomet - Compress Device Short Anchor Plug, 18 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement
FDA Device · Class II · 2023-11-29 · Biomet - Compress Device Short Anchor Plug, 24 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement
FDA Device · Class II · 2023-11-29 · Biomet - Compress Device Short Anchor Plug, 22 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement
FDA Device · Class II · 2023-11-29 · Biomet - Compress Device Short Anchor Plug, 26 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement
FDA Device · Class II · 2023-11-29 · Biomet - Compress Device Short Anchor Plug, 16 MM- Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement Item…
FDA Device · Class II · 2023-11-29 · Biomet - Compress Device Short Anchor Plug, 28 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement
FDA Device · Class II · 2023-11-29 · Biomet - Compress Device Segmental Anchor Plug, 10 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replaceme…
FDA Device · Class II · 2023-11-29 · Biomet - Compress Device Segmental Anchor Plug, 14 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replaceme…
FDA Device · Class II · 2023-11-29 · Biomet - Compress Device Short Anchor Plug, 23 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement
FDA Device · Class II · 2023-11-29 · Biomet - G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462
FDA Device · Class II · 2023-03-29 · Biomet - OSS Modular Arthrodesis Nail, 7 Degree Collar Assembly with Locking Bolts-For use in the replacement of segmental defects of long bone, inc…
FDA Device · Class II · 2023-02-08 · Biomet - (1) Vanguard Knee System PS Open Box Femoral
FDA Device · Class II · 2023-02-08 · Biomet - (1) Vanguard Knee System PS Open Box Femoral
FDA Device · Class II · 2023-02-08 · Biomet - Oxford Partial Knee System, Fixed Lateral Tibial Construct- Intended to replace part of a knee joint when used in conjunction with a femora…
FDA Device · Class II · 2023-02-01 · Biomet - BIOMET TRAUMA Drill Bit, Tap, Guide Pin: [DVR Drill Bit, Item # 212000022, DVR 2.2MM DRILL BIT], [ALPS Drill Bit, Item # 214227160, 2.7X160…
FDA Device · Class II · 2022-03-30 · Biomet - BIOMET Trauma, [Item # 13182-22-26, DVR CROSSLOCK EXTRA LONG PLATE LEFT], [Item # 1318-12-126, DVR CROSSLOCK EXTRA LONG PLATE RIGHT], [Item…
FDA Device · Class II · 2022-03-30 · Biomet - BIOMET Sports Medicine JUGGERLOC SLOTTED REAMER: [Item # 110010371, 6MM], [Item #110010372, 7MM], [Item # 110010373, 8MM], [Item #110018275…
FDA Device · Class II · 2022-03-30 · Biomet - BIOMET TRAUMA A.L.P.S. FIBULA COMPOSITE LOCKING PLATE 8 HOLE, Item # 856204008
FDA Device · Class II · 2022-03-30 · Biomet - Comprehensive Shoulder System Mini Humeral Stem, Porous Plasma, 12 MM, 83 MM Long Item Number: 113632
FDA Device · Class II · 2022-03-02 · Biomet - Comprehensive Shoulder System Primary Shoulder Stem, Micro Length, Porous Plasma, 11 MM, 55 MM Long Item Number: 113611
FDA Device · Class II · 2022-03-02 · Biomet - Comprehensive Shoulder System Primary Shoulder Stem, Micro Length, Porous Plasma, 14 MM, 55 MM Long Item Number: 113614
FDA Device · Class II · 2022-03-02 · Biomet - Arcos Modular Revision Hip System, Standard Cone Prox Body, Porous Plasma,Size A, 60 MM Item Number: 11-301301
FDA Device · Class II · 2022-03-02 · Biomet - Comprehensive Shoulder System Primary Shoulder Stem, Micro Length, Porous Plasma, 18 MM, 55 MM Long Item Number: 113618
FDA Device · Class II · 2022-03-02 · Biomet - Comprehensive Shoulder System Mini Humeral Stem, Porous Plasma, 11 MM, 83 MM Long Item Number: 113631
FDA Device · Class II · 2022-03-02 · Biomet - Comprehensive Shoulder System Mini Humeral Stem, Porous Plasma, 15 MM, 83 MM Long Item Number: 113635
FDA Device · Class II · 2022-03-02 · Biomet - Comprehensive Shoulder System Mini Humeral Stem, Porous Plasma, 13 MM, 83 MM Long Item Number: 113633
FDA Device · Class II · 2022-03-02 · Biomet - Arcos Modular Revision Hip System High Offset Cone Prox Body, Size E, 70 MM Item Number: 11-301335
FDA Device · Class II · 2021-08-18 · Biomet - Arcos Modular Revision Hip System Standard Cone Prox Body, Size B, 80 MM Item Number: 11-301342
FDA Device · Class II · 2021-08-18 · Biomet