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Endo-Model Modular Knee Prosthesis System 15-8521/09Recalls & reported problems

WALDEMAR LINK GmbH & Co. KG · Rotational Knee Joint Prosthesis,with anti-luxation device, condylus replacement · 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. Jan 12, 2026Class IIOpen, Classified

    The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

    Z-1518-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

  2. 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 ↗

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