Howmedica Osteonics Corp.
158 recalls on record · Latest: Dec 31, 2025
FDA Devices Moderate Dec 31, 2025
The Stryker CranialMask Tracker is a single-use device consisting of a flexible printed circuit board (PCB) with 31 infrared (IR) light-emitting diod…
FDA Devices Moderate Oct 8, 2025
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;
FDA Devices Moderate Oct 16, 2024
MAKO Integrated Cutting System (MICS) HANDPIECE, Catalog Number 209063
FDA Devices Moderate Oct 16, 2024
Triathlon Universal TS Baseplate Size 2 - A single use sterile implantable device intended for cemented applications during primary and revision Tota…
FDA Devices Moderate Sep 4, 2024
Custom Made Device - GMRS EXTENSION Piece 40MM LEFT, 35 Deg EXT Rotated Tabs (Patient Specific); Catalog Number: C-MM100434-00;
FDA Devices Moderate Jul 24, 2024
UNITRAX Endoprosthesis Head Component - 43mm. Implantable component used in partial hip arthroplasty. Catalog Number: 6942-5-043
FDA Devices Moderate Jul 24, 2024
UNITRAX Endoprosthesis Head Component - 38mm. Implantable component used in partial hip arthroplasty. Catalog Number: 6942-5-038
FDA Devices Moderate Jul 24, 2024
UNITRAX Endoprosthesis Head Component - 42mm. Implantable component used in partial hip arthroplasty. Catalog Number: 6942-5-042
FDA Devices Moderate Jun 26, 2024
Gray Revision Instrument System Accessory Tray/Case, Catalog/Part Number: 6210-9-910
FDA Devices Moderate Jun 26, 2024
HRIS Storage & Sterilization Case and Tray, Catalog/Part Number: 6210-9-900
FDA Devices Moderate May 1, 2024
TRIDENTII PSL CLUSTER58F-Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-58F
FDA Devices Moderate May 1, 2024
TRIDENTII PSL CLUSTER48D- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-48D
FDA Devices Moderate May 1, 2024
TRIDENTII HEMI CLUSTER66H- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-66H
FDA Devices Moderate May 1, 2024
TRIDENTII HEMI CLUSTER48D-indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-48D
FDA Devices Moderate May 1, 2024
TRIDENTII PSL CLUSTER52E- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-52E
FDA Devices Moderate May 1, 2024
TRIDENTII PSL CLUSTER64H- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-64H
FDA Devices Moderate May 1, 2024
TRIDENTII HEMI CLUSTER50D- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-50D
FDA Devices Moderate May 1, 2024
TRIDENTII HEMI CLUSTER52E-Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-52E
FDA Devices Moderate May 1, 2024
TRIDENTII HEMI CLUSTER58F- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-58F
FDA Devices Moderate Mar 13, 2024
NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM
FDA Devices Moderate Mar 13, 2024
X3 TRIATHLON CS INSERT NO 6 10 MM
FDA Devices Moderate Mar 13, 2024
X3 TRIATHLON CS INSERT NO 3 10 MM
FDA Devices Moderate Feb 14, 2024
HRIS ACET CUP CUT TIP 26X140 Part Number: 6210-5-100. single-use, sterile surgical instruments used during hip arthroplasty
FDA Devices Moderate Feb 7, 2024
Scorpio-Flex Ttl Kn P-S Tib Brg Insrt Asy- -Intended for knee replacement Part Number: 72-16-0910
FDA Devices Moderate Feb 7, 2024
PRIMARY REV.TIB.INSERT-DURACON Intended for knee replacement. Product Number: 6637-4-031
FDA Devices Moderate Feb 7, 2024
PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Product Number: 6742-1-411
FDA Devices Moderate Feb 7, 2024
SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #11 -Intended for knee replacement Part Number: 73-0110
FDA Devices Moderate Feb 7, 2024
LEFT SMALL-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement. Product Number: 6637-0-631
FDA Devices Moderate Feb 7, 2024
SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3710
FDA Devices Moderate Feb 7, 2024
SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #9 -Intended for knee replacement Part Number: 73-2910
FDA Devices Moderate Feb 7, 2024
SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #7 -Intended for knee replacement Part Number: 73-2710
FDA Devices Moderate Feb 7, 2024
SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3110
FDA Devices Moderate Feb 7, 2024
DURATION A-P LIPPED TIB.INSERT-DURAC Intended for knee replacement Product Number: 6642-1-911
FDA Devices Moderate Feb 7, 2024
SCORPIO RECESSED PATELLA- Intended for Knee Replacement Part Number: 3044-0026
FDA Devices Moderate Feb 7, 2024
SCORPIO RECESSED PATELLA- Intended for knee replacement Part Number: 3044-0028
FDA Devices Moderate Feb 7, 2024
SCORPIO RECESSED PATELLA-Intended for knee repalcment Part Number: 3044-0032
FDA Devices Moderate Feb 7, 2024
SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-0321
FDA Devices Moderate Feb 7, 2024
LEFT SMALL-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement Part Number: 6637-0-028
FDA Devices Moderate Feb 7, 2024
SCORPIO RECESSED PATELLA- Intended for knee replacement Part Number: 3044-0030
FDA Devices Moderate Feb 7, 2024
DUR PCA MTK REV INS LFT Intended for knee replacement Product Number: 6728-2-609
FDA Devices Moderate Feb 7, 2024
HOWMEDICA OSTEONICS TRIDENT 0 deg POLY INSERT Intended for knee replacement Part Number: 620-00-32J
FDA Devices Moderate Feb 7, 2024
SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #7 -Intended for knee replacement Part Number: 73-0710
FDA Devices Moderate Feb 7, 2024
SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #9 -Intended for knee replacement Part Number: 73-0910
FDA Devices Moderate Feb 7, 2024
DUR PCA MTK REV INS LFT Intended for knee replacement Product Number: 6728-2-611
FDA Devices Moderate Feb 7, 2024
SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3308
FDA Devices Moderate Feb 7, 2024
TIBIAL BEARING INSERT SERIES P-S I ASSY Intended for knee replacement Product Number: 7291-0324
FDA Devices Moderate Feb 7, 2024
PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Product Number: 6742-1-416
FDA Devices Moderate Feb 7, 2024
PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Product Number: 6742-1-413
FDA Devices Moderate Feb 7, 2024
SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-7514
FDA Devices Moderate Feb 7, 2024