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Endo-Model Standard Knee Prosthesis System 15-8024/11Recalls & reported problems

WALDEMAR LINK GmbH & Co. KG · Rotational Knee Joint Prosthesis,with anti-luxation device · Class 2 · Implant

All models of Endo-Model Standard Knee Prosthesis System (15)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04026575048045), received between Aug 25, 2023 and Aug 25, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Unclear 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 18, 2026.

Most reported problems

Device problems

  • Unclear Information1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionAug 25, 2023Unclear Information; Unclear Information

    WE HAVE IDENTIFIED A TRACEABILITY PROBLEM INTERNALLY, REGARDING THIS SERIAL NUMBER AND THE CORRESPONDING MARKING ON THE ITEM.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17623883 ↗

Other Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer devices

All Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page