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Unicondylar Sled Prosthesis 15-2020/52Recalls & reported problems

WALDEMAR LINK GmbH & Co. KG · Femoral Component · Class 2 · Implant

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

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
1

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04026575043903), received between Nov 7, 2024 and Oct 10, 2025 — classified as 2 injuries.

The most frequently reported specific device problem is “Fracture” (1 report).

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

31 other recalls cover devices cleared under the same FDA submission (K954186); 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. How this data works · Data updated Oct 13, 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: 1 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: 1 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Recalls naming this device

  1. Mar 21, 2023Open, Classified

    Additional Label Warnings: Amendment / reinforcement of the Surgical Technique and future product training on the updated technique, due to early aseptic loosening or increased wear of the implant caused by suboptimal positioning of the implant or inadequate cementing technique leading to an unsatisfactory surgical result, and in the worst case, intervention or revision earlier than expected

    Z-1509-2023 · Root cause: Labeling design · FDA record ↗

Most reported problems

Device problems

  • Fracture1
  • Loosening of Implant Not Related to Bone-Ingrowth1

Patient problems

  • Pain2
  • Failure of Implant1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryOct 10, 2025Loosening of Implant Not Related to Bone-Ingrowth; Loosening of Implant Not Related to Bone-Ingrowth

    REVISION DUE TO PAIN AND LOOSENING.

    Patient problems: Pain

    MAUDE report 23263999 ↗
  • InjuryNov 7, 2024Fracture; Fracture

    THE PATIENT HAS BEEN COMPLAINING ABOUT PAIN IN THE RIGHT KNEE JOINT. DURING THE REVISION SURGERY, THE BROKEN ENDOPROSTHESIS WAS DISCOVERED.

    Patient problems: Failure of Implant; Pain

    MAUDE report 20627962 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K954186. One submission often covers many models, so check the product and lot details in each record.

  • Z-1525-2023 · Mar 21, 2023 · Open, Classified
    LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 11X58MM Item Number: 15-2028/15
  • Z-1537-2023 · Mar 21, 2023 · Open, Classified
    LINK SLED Knee System ENDO MODEL SLED TIBIAL COMP 8 MM X 50 MM Item Number: 15-2030/14
  • Z-1523-2023 · Mar 21, 2023 · Open, Classified
    LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 7MM X 58MM Item Number: 15-2028/13
  • Z-1533-2023 · Mar 21, 2023 · Open, Classified
    LINK SLED Knee System ENDO MODEL SLED TIBIAL COMP 9 MM X 55 MM Item Number: 15-2030/10
  • Z-1510-2023 · Mar 21, 2023 · Open, Classified
    LINK SLED Knee System: ENDO SLED KNEE FEM COMP, Large Item Number: 15-2020/60
  • Z-1514-2023 · Mar 21, 2023 · Open, Classified
    LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 13MM X 45MM Item Number: 15-2028/04
  • Z-1512-2023 · Mar 21, 2023 · Open, Classified
    LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 9MM X 45MM Item Number: 15-2028/02
  • Z-1529-2023 · Mar 21, 2023 · Open, Classified
    LINK SLED Knee System ENDO MODEL SLED TIBIAL COMP 13 MM X 45 MM Item Number: 15-2030/04
  • Z-1538-2023 · Mar 21, 2023 · Open, Classified
    LINK SLED Knee System ENDO MODEL SLED TIBIAL COMP 8 MM X 55 MM Item Number: 15-2030/15
  • Z-1532-2023 · Mar 21, 2023 · Open, Classified
    LINK SLED Knee System ENDO MODEL SLED TIBIAL COMP 13 MM X 50 MM Item Number: 15-2030/08
  • Z-1511-2023 · Mar 21, 2023 · Open, Classified
    LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 7MM X 45MM Item Number: 15-2028/01
  • Z-1530-2023 · Mar 21, 2023 · Open, Classified
    LINK SLED Knee System ENDO MODEL SLED TIBIAL COMP 9 MM X 50 MM Item Number: 15-2030/06
  • Z-1528-2023 · Mar 21, 2023 · Open, Classified
    LINK SLED Knee System: ENDO MODEL SLED TIBIAL COMP 11 MM X 45 MM Item Number: 15-2030/03
  • Z-1520-2023 · Mar 21, 2023 · Open, Classified
    LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 9MM X 55MM Item Number: 15-2028/10
  • Z-1507-2023 · Mar 21, 2023 · Open, Classified
    LINK SLED Knee System: ENDO SLED KNEE FEM COMP, SMALL Item Number: 15-2020/40

…and 16 more.

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

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

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.