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Howmedica Osteonics Corp. Recalls

152 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Howmedica Osteonics Corp..

152Total Recalls
0Critical
98,487Units Affected
Feb 2, 2026Most Recent
All Recalls

Every Howmedica Osteonics Corp. Recall

Sorted by most recent. Click any recall for full details.

152 recalls
High RiskFDA
Howmedica Osteonics Corp.
MICS3 Angled Sagittal Saw Attachment; Part Number: 210490
Medical Devices·1,098 affected·Feb 2, 2026
High RiskFDA
Howmedica Osteonics Corp.
The Stryker CranialMask Tracker is a single-use device consisting of a flexible printed circuit board (PCB) with 31 infrared (IR) light-e...
Medical Devices·320 affected·Nov 12, 2025
High RiskFDA
Howmedica Osteonics Corp.
1. EXETER V40 STEM 44MM NO 2, Model/Catalog Number: 0580-1-442; 2. EXETER V40 STEM 37.5MM NO 0, Model/Catalog Number: 0580-1-352;
Medical Devices·55 affected·Aug 28, 2025
High RiskFDA
Howmedica Osteonics Corp.
Triathlon Universal TS Baseplate Size 2 - A single use sterile implantable device intended for cemented applications during primary and r...
Medical Implants·16 affected·Sep 4, 2024
High RiskFDA
Howmedica Osteonics Corp.
MAKO Integrated Cutting System (MICS) HANDPIECE, Catalog Number 209063
Medical Devices·897 affected·Aug 7, 2024
High RiskFDA
Howmedica Osteonics Corp.
Custom Made Device - GMRS EXTENSION Piece 40MM LEFT, 35 Deg EXT Rotated Tabs (Patient Specific); Catalog Number: C-MM100434-00;
Medical Devices·1 affected·Aug 5, 2024
High RiskFDA
Howmedica Osteonics Corp.
UNITRAX Endoprosthesis Head Component - 43mm. Implantable component used in partial hip arthroplasty. Catalog Number: 6942-5-043
Medical Implants·18 affected·Jun 19, 2024
High RiskFDA
Howmedica Osteonics Corp.
UNITRAX Endoprosthesis Head Component - 38mm. Implantable component used in partial hip arthroplasty. Catalog Number: 6942-5-038
Medical Implants·12 affected·Jun 19, 2024
High RiskFDA
Howmedica Osteonics Corp.
UNITRAX Endoprosthesis Head Component - 42mm. Implantable component used in partial hip arthroplasty. Catalog Number: 6942-5-042
Medical Implants·18 affected·Jun 19, 2024
High RiskFDA
Howmedica Osteonics Corp.
Gray Revision Instrument System Accessory Tray/Case, Catalog/Part Number: 6210-9-910
Medical Devices·209 affected·May 23, 2024
High RiskFDA
Howmedica Osteonics Corp.
HRIS Storage & Sterilization Case and Tray, Catalog/Part Number: 6210-9-900
Medical Devices·630 affected·May 23, 2024
High RiskFDA
Howmedica Osteonics Corp.
TRIDENTII PSL CLUSTER58F-Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-1...
Medical Devices·0 affected·Feb 27, 2024
High RiskFDA
Howmedica Osteonics Corp.
TRIDENTII PSL CLUSTER48D- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-48D
Medical Devices·0 affected·Feb 27, 2024
High RiskFDA
Howmedica Osteonics Corp.
TRIDENTII HEMI CLUSTER66H- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-66H
Medical Devices·0 affected·Feb 27, 2024
High RiskFDA
Howmedica Osteonics Corp.
TRIDENTII HEMI CLUSTER48D-indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-48D
Medical Devices·45 affected·Feb 27, 2024
High RiskFDA
Howmedica Osteonics Corp.
TRIDENTII PSL CLUSTER52E- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-52E
Medical Devices·3 affected·Feb 27, 2024
High RiskFDA
Howmedica Osteonics Corp.
TRIDENTII PSL CLUSTER64H- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-64H
Medical Devices·0 affected·Feb 27, 2024
High RiskFDA
Howmedica Osteonics Corp.
TRIDENTII HEMI CLUSTER50D- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-50D
Medical Devices·0 affected·Feb 27, 2024
High RiskFDA
Howmedica Osteonics Corp.
TRIDENTII HEMI CLUSTER52E-Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-52E
Medical Devices·48 affected·Feb 27, 2024
High RiskFDA
Howmedica Osteonics Corp.
TRIDENTII HEMI CLUSTER58F- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-58F
Medical Devices·0 affected·Feb 27, 2024
High RiskFDA
Howmedica Osteonics Corp.
NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM
Medical Devices·18 affected·Feb 6, 2024
High RiskFDA
Howmedica Osteonics Corp.
X3 TRIATHLON CS INSERT NO 6 10 MM
Medical Devices·143 affected·Feb 6, 2024
High RiskFDA
Howmedica Osteonics Corp.
X3 TRIATHLON CS INSERT NO 3 10 MM
Medical Devices·132 affected·Feb 6, 2024
High RiskFDA
Howmedica Osteonics Corp.
HRIS ACET CUP CUT TIP 26X140 Part Number: 6210-5-100. single-use, sterile surgical instruments used during hip arthroplasty
Surgical Devices·0 affected·Dec 22, 2023
High RiskFDA
Howmedica Osteonics Corp.
Scorpio-Flex Ttl Kn P-S Tib Brg Insrt Asy- -Intended for knee replacement Part Number: 72-16-0910
Medical Devices·9 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
PRIMARY REV.TIB.INSERT-DURACON Intended for knee replacement. Product Number: 6637-4-031
Medical Devices·0 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Product Number: 6742-1-411
Medical Devices·0 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #11 -Intended for knee replacement Part Number: 73-0110
Medical Devices·61 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
LEFT SMALL-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement. Product Number: 6637-0-631
Medical Devices·0 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3710
Medical Devices·118 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #9 -Intended for knee replacement Part Number: 73-2910
Medical Devices·16 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #7 -Intended for knee replacement Part Number: 73-2710
Medical Devices·36 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3110
Medical Devices·107 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
DURATION A-P LIPPED TIB.INSERT-DURAC Intended for knee replacement Product Number: 6642-1-911
Medical Devices·0 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO RECESSED PATELLA- Intended for Knee Replacement Part Number: 3044-0026
Medical Devices·94 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO RECESSED PATELLA- Intended for knee replacement Part Number: 3044-0028
Medical Devices·52 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO RECESSED PATELLA-Intended for knee repalcment Part Number: 3044-0032
Medical Devices·70 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-0321
Medical Devices·0 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
LEFT SMALL-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement Part Number: 6637-0-028
Medical Devices·0 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO RECESSED PATELLA- Intended for knee replacement Part Number: 3044-0030
Medical Devices·77 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
DUR PCA MTK REV INS LFT Intended for knee replacement Product Number: 6728-2-609
Medical Devices·0 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
HOWMEDICA OSTEONICS TRIDENT 0 deg POLY INSERT Intended for knee replacement Part Number: 620-00-32J
Medical Devices·0 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #7 -Intended for knee replacement Part Number: 73-0710
Medical Devices·269 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #9 -Intended for knee replacement Part Number: 73-0910
Medical Devices·192 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
DUR PCA MTK REV INS LFT Intended for knee replacement Product Number: 6728-2-611
Medical Devices·0 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3308
Medical Devices·1 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
TIBIAL BEARING INSERT SERIES P-S I ASSY Intended for knee replacement Product Number: 7291-0324
Medical Devices·0 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Product Number: 6742-1-416
Medical Devices·0 affected·Dec 1, 2023