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Duracon 6642-2-626Recalls & reported problems

Howmedica Osteonics Corp. · Inset Patella · Class 2 · Implant

All models of Duracon (58)

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

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613153132738), received between Jul 2, 2018 and Jul 2, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).

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.

Most reported problems

Device problems

  • Insufficient Device Problem Information1

Patient problems

  • Injury1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryJul 2, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

    PATIENT HAD RIGHT KNEE SURGERY DONE ON (B)(6) 2013 AND WAS REVISED ON (B)(6) 2018 DUE TO LITTLE BONE GROWTH. PATIENT WAS REVISED TO NON STRYKER IMPLANTS.

    Patient problems: Injury

    MAUDE report 7654918 ↗

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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