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Endo-Model Modular Knee Prosthesis System 15-2979/01Recalls & reported problems

WALDEMAR LINK GmbH & Co. KG · Femoral Segment,Size 4 · Class 2 · Implant

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

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04026575328093), received between Jul 28, 2023 and Jul 28, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Component or Accessory Incompatibility” (1 report).

1 FDA recall record name this device's identifier, 1 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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Mar 18, 2021Open, Classified

    The firm discovered through customer complaints that device segments may not meet specifications.

    Z-2048-2023 · Root cause: Device Design · FDA record ↗

Most reported problems

Device problems

  • Component or Accessory Incompatibility1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionJul 28, 2023Component or Accessory Incompatibility; Component or Accessory Incompatibility

    . DIFFICULT OR DELAYED POSITIONING OF FEMORAL SEGMENT [CUSTOMER].

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17413428 ↗

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

All Prosthesis, Knee, Femorotibial, 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.