Howmedica Osteonics recalls

Howmedica Osteonics appears in 232 official U.S. recall notices indexed by RecallRadar, most recently on 2026-06-24.

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

• 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
• HRIS ACET CUP CUT TIP 26X140 Part Number: 6210-5-100. single-use, sterile surgical instruments used during hip arthroplasty
  FDA Device · Class II · 2024-02-14 · Howmedica Osteonics
• Scorpio-Flex Ttl Kn P-S Tib Brg Insrt Asy- -Intended for knee replacement Part Number: 72-16-0910
  FDA Device · Class II · 2024-02-07 · Howmedica Osteonics
• SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-0321
  FDA Device · Class II · 2024-02-07 · Howmedica Osteonics
• PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Product Number: 6742-1-413
  FDA Device · Class II · 2024-02-07 · Howmedica Osteonics
• PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Product Number: 6742-1-416
  FDA Device · Class II · 2024-02-07 · Howmedica Osteonics
• DUR PCA MTK REV INS RT Intended for knee replacement Product Number: 6728-2-711
  FDA Device · Class II · 2024-02-07 · Howmedica Osteonics
• RGT.LARGE-PCA MOD.REV.- DUR.REV.INSERT Intended for knee replacement
  FDA Device · Class II · 2024-02-07 · Howmedica Osteonics
• HOWMEDICA OSTEONICS TRIDENT 0 deg POLY INSERT Intended for knee replacement Part Number: 620-00-32J
  FDA Device · Class II · 2024-02-07 · Howmedica Osteonics
• LEFT SMALL-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement Part Number: 6637-0-028
  FDA Device · Class II · 2024-02-07 · Howmedica Osteonics
• SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-7521
  FDA Device · Class II · 2024-02-07 · Howmedica Osteonics
• SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #7 -Intended for knee replacement Part Number: 73-2710
  FDA Device · Class II · 2024-02-07 · Howmedica Osteonics
• DURATION PLASTIC PATELLA-DURACON Intended for knee replacement Product Number: 6642-2-200
  FDA Device · Class II · 2024-02-07 · Howmedica Osteonics
• SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3708
  FDA Device · Class II · 2024-02-07 · Howmedica Osteonics
• LEFT X-LARGE-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement
  FDA Device · Class II · 2024-02-07 · Howmedica Osteonics
• SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3710
  FDA Device · Class II · 2024-02-07 · Howmedica Osteonics
• LARGE PRIMARY REV.TIB.INSERT- DURACON Intended for knee replacement Product Number: 6637-4-231
  FDA Device · Class II · 2024-02-07 · Howmedica Osteonics