Howmedica Osteonics Corp
325 CORPORATE DR., MAHWAH, NJ, US
Registered product codes
64 product codes
Recent MDR events
609 on file
- CENTPILLAR TMZF RIGHT, SIZE 6Jul 14, 2026InjuryMW5190711
- RESTORATION STEMJul 10, 2026InjuryMW5190574
- CERAMIC V40 FEMORAL HOSPITALJul 6, 2026MalfunctionMW5190227
- 2.5 I M PLUGJul 6, 2026MalfunctionMW5190228
- V40 STEMJul 6, 2026MalfunctionMW5190229
- 6 CS 9 MM TIBIAL TRIALJun 29, 2026InjuryMW5189975
- STRYKER SH BASEPLATE NUMBER 4 TIBIALJun 23, 2026OtherMW5189818
- DRILL BIT SIZE 2.5Jun 11, 2026InjuryMW5189332
- TRIATHLON KNEE REPLACEMENTJun 11, 2026InjuryMW5189350
- STRYKER CUPJun 11, 2026InjuryMW5189374
Recalls
741 on file
- Open, ClassifiedJun 17, 2026
Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon Universal Baseplate Size 4 (lot TYX7OB), is contained in packaging labeled as Triathlon Universal Baseplate Size 3, (lot UZD9IB).
View FDA record ↗ - Open, ClassifiedJun 17, 2026
Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon Universal Baseplate Size 4 (lot TYX7OB), is contained in packaging labeled as Triathlon Universal Baseplate Size 3, (lot UZD9IB).
View FDA record ↗ - Open, ClassifiedMar 18, 2026
A potential issue was identified with the torque strength on the external screws of the MICS3 Angled Sagittal Saw Attachment. These screws, which secure the cover to the Angled Saw Housing, may loosen during use and detach from the attachment.
View FDA record ↗ - Open, ClassifiedDec 19, 2025
When the device is activated during surgery, the device software issues an error message "Instrument Face Mask (6001385000000) is not valid for this application" resulting in an inability to use the device.
View FDA record ↗ - Open, ClassifiedSep 26, 2025
a potential product mix where the package labeled as Catalog Number 0580-1-442, lot A00976, may contain Catalog Number 0580-1-352, lot G8754849, and vice versa. Patient labels may also be impacted.
View FDA record ↗ - Open, ClassifiedOct 9, 2024
Stryker has identified an issue with the characterization process that impacted the constant values assigned to the associated MICS Handpieces.
View FDA record ↗ - Open, ClassifiedOct 7, 2024
Anterior locking tabs on the Triathlon Universal Baseplate are out of specification which may prevent engagement of either of the two locking tabs with the locking wire of the tibial insert.
View FDA record ↗ - Open, ClassifiedAug 26, 2024
A patient specific, custom-made device was supplied for a surgical procedure that did not match the design proposal.
View FDA record ↗ - Open, ClassifiedJul 16, 2024
Mislabeled: the size on the package label of the UNITRAX Endoprosthesis Head Component potentially may not match the device within the packaging. This product mix only involves the three (3) sizes (43mm, 42mm, and the 38mm)
View FDA record ↗ - Open, ClassifiedJul 16, 2024
Mislabeled: the size on the package label of the UNITRAX Endoprosthesis Head Component potentially may not match the device within the packaging. This product mix only involves the three (3) sizes (43mm, 42mm, and the 38mm)
View FDA record ↗
Compliance history
Matched by FEI 3003070421.
FDA inspections
1 on file
- Voluntary Action Indicated (VAI)Dec 1, 2023
Compliance: Devices · Citations posted
Inspection citations
1 on file
Top cited requirements
Compare to industry ↗- 21 CFR 820.25(b)Dec 1, 2023
Training - Lack of or inadequate procedures
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.