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Endo-Model Modular Knee Prosthesis System 15-2816/11Recalls & reported problems

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

Data updated Oct 13, 2026 from official FDA records · Editorial policy

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

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

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. May 22, 2024Open, Classified

    Blind screws of the modular tibial component cannot be loosened intraoperatively,prolongation surgery due to intraoperatively change in procedure, probably to cementing technique

    Z-2410-2024 · Root cause: Process design · FDA record ↗

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