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Endo-Model Modular Knee Prosthesis System 15-2814/04Recalls & reported problems

WALDEMAR LINK GmbH & Co. KG · Rotational Knee Joint Prosthesis,Tibial component · Class 2 · Implant

All models of Endo-Model Modular Knee Prosthesis System (64)

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

2 open recalls name 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
2

Summary

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

2 FDA recall records name this device's identifier, 2 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

  1. May 22, 2024Class IIOpen, 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 · Recall details · FDA record ↗

  2. May 24, 2022Class IIOpen, Classified

    There is a risk that blind screws of the modular tibial component cannot be loosened intraoperatively. This may lead to prolongation of surgery due to an intraoperative change in procedure.

    Z-1377-2022 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗

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

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

Sources and updates

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