Howmedica Osteonics recalls

Howmedica Osteonics appears in 248 official U.S. recall notices indexed by RecallRadar, most recently on 2026-10-21.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• TS Femoral Prep Tray, Triathlon
  FDA Device · Class II · 2026-10-21 · Howmedica Osteonics
• TS Misc
  FDA Device · Class II · 2026-10-21 · Howmedica Osteonics
• TS Universal Baseplate Finishing Tray, Triathlon
  FDA Device · Class II · 2026-10-21 · Howmedica Osteonics
• Triathlon Hinge Femoral Prep Tray
  FDA Device · Class II · 2026-10-21 · Howmedica Osteonics
• BEARING AND AXLE BUSHING ASSY STD ELBOW C-M113-1-301 KRH REV TIB INS 16mm THK .640 DIA STEM C-M113-5-600 SELF-PRESSURIZING GLENOID SIZE 9 C…
  FDA Device · Class II · 2026-09-23 · Howmedica Osteonics
• TRIATHLON HINGE INSERT SIZE 4 11MM 5612-P-411 TRIATHLON HINGE INSERT SIZE 4 13MM 5612-P-413 Orthopaedic implant components manufactured fro…
  FDA Device · Class II · 2026-09-23 · Howmedica Osteonics
• SCORPIO C-DOME PATELLA 73-2710 73-2910 SCORPIO U-DOME PATELLA 73-3110 73-3508 73-3708 73-3710 73-3910 Orthopaedic implant components manufa…
  FDA Device · Class II · 2026-09-23 · Howmedica Osteonics
• DURACON XL ANGLED TIB INS 11/14MM C-M064-1-300 SELF-PRESSURIZING GLENOID SIZE 8 C-M062-6-800 C-M062-7-500 C-M063-2-600 SELF-PRESSURIZING GL…
  FDA Device · Class II · 2026-09-23 · Howmedica Osteonics
• AXLE PIN ASSY LARGE ELBOW COBALT CHROME Catalog No. C-M112-2-500 Orthopaedic implant components manufactured from UHMWPE (polyethylene)
  FDA Device · Class II · 2026-09-23 · Howmedica Osteonics
• SCORPIO + MOBILE BEARING PCS 78-5-0910 SYSTEM ONE BIPOLAR 40MM 6074-4022 SYSTEM ONE BIPOLAR 43MM 6074-4322 SYSTEM ONE BIPOLAR 44MM 6074-442…
  FDA Device · Class II · 2026-09-23 · Howmedica Osteonics
• ALL POLY CONSTRAINED INSERT 54MM 69-2854 NRG KNEE CR 82-2-0512 82-2-0518 82-2-0912 NRG KNEE P/S 82-3-0318 SCORPIO + MOBILE BEARING PCS 78-5…
  FDA Device · Class II · 2026-09-23 · Howmedica Osteonics
• SCORPIO RECESSED METAL BACKED PATELLA 3045-0026 3045-0028 3045-0030 3045-0032 Orthopaedic implant components manufactured from UHMWPE (poly…
  FDA Device · Class II · 2026-09-23 · Howmedica Osteonics
• ACETABULAR CUP UHMWPE 61-3258 ALL POLY CONSTRAINED INSERT 44MM 69-2244 ALL POLY CONSTRAINED INSERT 46MM 69-2246 ALL POLY CONSTRAINED INSERT…
  FDA Device · Class II · 2026-09-23 · Howmedica Osteonics
• OMNIFIT SERIES I ACET. INSERT 10¿ 22mm ID Catalog No. 2001-2246 Orthopaedic implant components manufactured from UHMWPE (polyethylene)
  FDA Device · Class II · 2026-09-23 · Howmedica Osteonics
• ABG I ACETABULAR INSERT HOODED 28mm ID X 48mm C-M079-2-801 ARC2F ACETABULAR INSERT 48/50/52mm OD x 28mm ID C-M071-6-700 ARC2F ACETABULAR IN…
  FDA Device · Class II · 2026-09-23 · Howmedica Osteonics
• TRIDENT 0¿ POLY INSERT 28mm ID 620-00-28D Orthopaedic implant components manufactured from UHMWPE (polyethylene)
  FDA Device · Class II · 2026-09-23 · Howmedica Osteonics
• TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400
  FDA Device · Class II · 2026-06-24 · Howmedica Osteonics
• TRI TS BASEPLATE SIZE 3. Part Number: 5521-B-300
  FDA Device · Class II · 2026-06-24 · Howmedica Osteonics
• MICS3 Angled Sagittal Saw Attachment
  FDA Device · Class II · 2026-03-25 · Howmedica Osteonics
• The Stryker CranialMask Tracker is a single-use device consisting of a flexible printed circuit board (PCB) with 31 infrared (IR) light-emi…
  FDA Device · Class II · 2025-12-31 · Howmedica Osteonics
• 1. EXETER V40 STEM 44MM NO 2, Model/Catalog Number: 0580-1-442
  FDA Device · Class II · 2025-10-08 · Howmedica Osteonics
• Triathlon Universal TS Baseplate Size 2 - A single use sterile implantable device intended for cemented applications during primary and rev…
  FDA Device · Class II · 2024-10-16 · Howmedica Osteonics
• MAKO Integrated Cutting System (MICS) HANDPIECE, Catalog Number 209063
  FDA Device · Class II · 2024-10-16 · Howmedica Osteonics
• Custom Made Device - GMRS EXTENSION Piece 40MM LEFT, 35 Deg EXT Rotated Tabs (Patient Specific)
  FDA Device · Class II · 2024-09-04 · Howmedica Osteonics
• UNITRAX Endoprosthesis Head Component - 43mm
  FDA Device · Class II · 2024-07-24 · Howmedica Osteonics
• UNITRAX Endoprosthesis Head Component - 42mm
  FDA Device · Class II · 2024-07-24 · Howmedica Osteonics
• UNITRAX Endoprosthesis Head Component - 38mm
  FDA Device · Class II · 2024-07-24 · Howmedica Osteonics
• HRIS Storage & Sterilization Case and Tray, Catalog/Part Number: 6210-9-900
  FDA Device · Class II · 2024-06-26 · Howmedica Osteonics
• Gray Revision Instrument System Accessory Tray/Case, Catalog/Part Number: 6210-9-910
  FDA Device · Class II · 2024-06-26 · Howmedica Osteonics
• TRIDENTII PSL CLUSTER48D- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-48D
  FDA Device · Class II · 2024-05-01 · Howmedica Osteonics
• TRIDENTII HEMI CLUSTER52E-Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-52E
  FDA Device · Class II · 2024-05-01 · Howmedica Osteonics
• TRIDENTII HEMI CLUSTER54E- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-54E
  FDA Device · Class II · 2024-05-01 · Howmedica Osteonics
• TRIDENTII PSL CLUSTER52E- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-52E
  FDA Device · Class II · 2024-05-01 · Howmedica Osteonics
• TRIDENTII HEMI CLUSTER58F- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-58F
  FDA Device · Class II · 2024-05-01 · Howmedica Osteonics
• TRIDENTII PSL CLUSTER50D- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-50D
  FDA Device · Class II · 2024-05-01 · Howmedica Osteonics
• TRIDENTII HEMI CLUSTER44B- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-44B
  FDA Device · Class II · 2024-05-01 · Howmedica Osteonics
• TRIDENTII PSL CLUSTER64H- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-64H
  FDA Device · Class II · 2024-05-01 · Howmedica Osteonics
• TRIDENTII HEMI CLUSTER48D-indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-48D
  FDA Device · Class II · 2024-05-01 · Howmedica Osteonics
• TRIDENTII HEMI CLUSTER66H- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-66H
  FDA Device · Class II · 2024-05-01 · Howmedica Osteonics
• TRIDENTII PSL CLUSTER58F-Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-58F
  FDA Device · Class II · 2024-05-01 · Howmedica Osteonics
• TRIDENTII HEMI CLUSTER50D- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-50D
  FDA Device · Class II · 2024-05-01 · Howmedica Osteonics
• X3 TRIATHLON CS INSERT NO 6 10 MM
  FDA Device · Class II · 2024-03-13 · Howmedica Osteonics
• X3 TRIATHLON CS INSERT NO 7 9 MM
  FDA Device · Class II · 2024-03-13 · Howmedica Osteonics
• NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM
  FDA Device · Class II · 2024-03-13 · Howmedica Osteonics
• NO 3 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM
  FDA Device · Class II · 2024-03-13 · Howmedica Osteonics
• NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 16 MM
  FDA Device · Class II · 2024-03-13 · Howmedica Osteonics
• X3 TRIATHLON CS INSERT NO 6 11 MM
  FDA Device · Class II · 2024-03-13 · Howmedica Osteonics
• X3 TRIATHLON CS INSERT NO 3 10 MM
  FDA Device · Class II · 2024-03-13 · Howmedica Osteonics
• NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 16 MM
  FDA Device · Class II · 2024-03-13 · Howmedica Osteonics
• HRIS ACET CUP CUT TIP 32X140 Part Number: 6210-5-200rker. single-use, sterile surgical instruments used during hip arthroplasty
  FDA Device · Class II · 2024-02-14 · Howmedica Osteonics