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Triathlon 5530-G-511-ERecalls & reported problems

Howmedica Osteonics Corp. · Tibial Bearing Insert - CR · Class 2 · Implant

All models of Triathlon (608)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327382846), received between Jul 22, 2021 and Oct 9, 2023 — classified as 2 injuries.

The most frequently reported specific device problem is “Degraded” (1 report).

7 other recalls cover devices cleared under the same FDA submission (K172634); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem2
  • Degraded1

Patient problems

  • Unspecified Infection1
  • Wound Dehiscence1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryOct 9, 2023Degraded; Adverse Event Without Identified Device or Use Problem; Degraded; Adverse Event Without Identified Device or Use Problem

    RE-OPR DUE TO COMPLICATIONS WITH WOUND CLOSURE. ADDITIONAL INFORMATION: UNDER THE OPR SURGEON FOUND SCRATCH MARKS ON THE SURFACE OF THE INSERT.

    Patient problems: Wound Dehiscence

    MAUDE report 17894140 ↗
  • InjuryJul 22, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE PATIENT'S RIGHT KNEE WAS REVISED DUE TO POSSIBLE INFECTION. A 5X11 CR INSERT WAS REVISED. REP CONFIRMED THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.

    Patient problems: Unspecified Infection

    MAUDE report 12211605 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K172634. One submission often covers many models, so check the product and lot details in each record.

  • Z-1265-2024 · Feb 6, 2024 · Open, Classified
    NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 16 MM
  • Z-1264-2024 · Feb 6, 2024 · Open, Classified
    NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM
  • Z-1262-2024 · Feb 6, 2024 · Open, Classified
    X3 TRIATHLON CS INSERT NO 7 9 MM
  • Z-1266-2024 · Feb 6, 2024 · Open, Classified
    NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 16 MM
  • Z-1263-2024 · Feb 6, 2024 · Open, Classified
    NO 3 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM
  • Z-1261-2024 · Feb 6, 2024 · Open, Classified
    X3 TRIATHLON CS INSERT NO 6 11 MM
  • Z-1654-2023 · Apr 13, 2023 · Open, Classified
    TRIATHLON X3 TIBIAL BEARING INSERT PS #4 13MM Intended for knee replacement Catalog Number: 5532-G-413-E

Other PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER devices

All PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER devices →

Sources and updates

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