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Modular Stem, 15-8522/40Recalls & reported problems

WALDEMAR LINK GmbH & Co. KG · Modular Stem, · Class 2 · Implant

Data updated Oct 16, 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 04026575381777), received between Jun 18, 2026 and Jun 18, 2026 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (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 16, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 1 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Fracture1

Patient problems

  • Periprosthetic fracture1

Recent adverse event reports

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

  • InjuryJun 18, 2026Fracture

    FRACTURE OF THE FEMORAL STEM [CUSTOMER]

    Patient problems: Periprosthetic fracture

    MAUDE report 25547759 ↗

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-1520-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model Replacement Plateau; Item Number: 15-8521/15;
  • Z-1517-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model Replacement Plateau; Item Number: 15-8030/12;
  • Z-1522-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model Replacement Plateau; Item Number: 15-0027/12;
  • Z-1523-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model Replacement Plateau; Item Number: 15-0027/16;
  • Z-1513-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/02;
  • Z-1519-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model Replacement Plateau; Item Number: 15-8521/11;
  • Z-1515-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model Replacement Plateau; Item Number: 15-2835/12;
  • Z-1512-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model Replacement Plateau; Item Number: 15-0027/15;
  • Z-1511-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/05;
  • Z-1521-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model Replacement Plateau; Item Number: 15-0027/11;
  • Z-1514-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/07;
  • Z-1516-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model Replacement Plateau; Item Number: 15-2836/11;
  • Z-1518-2026 · Jan 12, 2026 · Open, Classified
    Endo-Model Replacement Plateau; Item Number: 15-8521/09;
  • 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

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