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Endo-Model SL Knee Prosthesis System 15-8515/55Recalls & reported problems

WALDEMAR LINK GmbH & Co. KG · Modular Stem,with femoral traper and 6 mm noses · Class 2 · Implant

All models of Endo-Model SL Knee Prosthesis System (25)

Data updated Oct 18, 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 04026575384006), received between Jan 16, 2023 and Jan 16, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Loosening of Implant Not Related to Bone-Ingrowth” (1 report).

16 other recalls cover devices cleared under the same FDA submission (K151008); they may or may not involve this specific model.

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

  • Loosening of Implant Not Related to Bone-Ingrowth1
  • Osseointegration Problem1

Patient problems

  • Failure of Implant1

Recent adverse event reports

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

  • InjuryJan 16, 2023Osseointegration Problem; Loosening of Implant Not Related to Bone-Ingrowth; Osseointegration Problem; Loosening of Implant Not Related to Bone-Ingrowth

    THE PATIENT HAD UNDERGONE SEVERAL PRIOR REVISIONS FOLLOWING REVISION TOTAL KNEE REPLACEMENT PERFORMED IN (B)(6) 2016, WITH PRECEDING HISTORY OR LIMB SALVAGE SURGERY AND INFECTED TOTAL KNEE ARTHROPLASTY. THIS TIBIAL TRAY AND STEM (IMPLANTED IN 2021) WERE REVISED TO A CUSTOM-MADE IMPLANT. PER DR. M., THE CAUSE OF THE LOOSENED TIBIA WAS "TERRIBLE BONE STOCK. TOO SMALL A DIAMETER STEM AND PROBABLY NOT LONG ENOUGH AS WELL."

    Patient problems: Failure of Implant

    MAUDE report 16172827 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K151008. One submission often covers many models, so check the product and lot details in each record.

  • Z-1514-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/07;
  • Z-1522-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model Replacement Plateau; Item Number: 15-0027/12;
  • Z-1511-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/05;
  • Z-1515-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model Replacement Plateau; Item Number: 15-2835/12;
  • Z-1521-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model Replacement Plateau; Item Number: 15-0027/11;
  • Z-1513-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/02;
  • Z-1512-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model Replacement Plateau; Item Number: 15-0027/15;
  • Z-1520-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model Replacement Plateau; Item Number: 15-8521/15;
  • Z-1519-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model Replacement Plateau; Item Number: 15-8521/11;
  • Z-1518-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model Replacement Plateau; Item Number: 15-8521/09;
  • Z-1516-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model Replacement Plateau; Item Number: 15-2836/11;
  • Z-1517-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model Replacement Plateau; Item Number: 15-8030/12;
  • Z-1523-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model Replacement Plateau; Item Number: 15-0027/16;
  • Z-0890-2026 · Nov 10, 2025 · Open, Classified
    Endo Model Knee Fusion Nail SK, Knee Fusion Nail, Coupling Component, right, modular, L= 68 mm, Taper 10/12. Knee component of limb salvage replacement devices.
  • Z-2410-2024 · May 22, 2024 · Open, Classified
    Endo Model M Tibial Components Modular Knee Prosthesis System. Product codes 15-2814/01, 15-2814/02, 15-2814/03, 15-2814/04, 15-2815/11, 15-2815/12, 15-2816/11, 15-2816/12, 15-281

…and 1 more.

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

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Sources and updates

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