Endo-Model Standard Knee Prosthesis System 16-2011/21Recalls & reported problems
WALDEMAR LINK GmbH & Co. KG · Sparepart Kit Boxes for Endo-Model SL · Class 2 · Implant
All models of Endo-Model Standard Knee Prosthesis System (15)
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 04026575222049), received between Mar 22, 2023 and Mar 22, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Positioning Failure” (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
- Positioning Failure1
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.
InjuryMar 22, 2023Positioning Failure; Positioning Failure
AXIS DID NOT FIT INTO BEARING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16588891 ↗
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-1517-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model Replacement Plateau; Item Number: 15-8030/12;
- Z-1519-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model Replacement Plateau; Item Number: 15-8521/11;
- Z-1511-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/05;
- Z-1522-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model Replacement Plateau; Item Number: 15-0027/12;
- Z-1523-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model Replacement Plateau; Item Number: 15-0027/16;
- Z-1520-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model Replacement Plateau; Item Number: 15-8521/15;
- Z-1521-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model Replacement Plateau; Item Number: 15-0027/11;
- Z-1516-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model Replacement Plateau; Item Number: 15-2836/11;
- Z-1518-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model Replacement Plateau; Item Number: 15-8521/09;
- Z-1515-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model Replacement Plateau; Item Number: 15-2835/12;
- Z-1512-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model Replacement Plateau; Item Number: 15-0027/15;
- Z-1514-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/07;
- Z-1513-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/02;
- Z-0890-2026 · Nov 10, 2025 · Open, ClassifiedEndo 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, ClassifiedEndo 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, hip, semi-constrained, metal/polymer, cemented devices
- NA 1365-51-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented753 reports
- NA 1365-50-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented412 reports
- ARTICUL/EZE 1365-21-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall280 reports
- ARTICUL/EZE 1365-11-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 death262 reports
- LFIT 6260-9-236Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, cemented256 reports
- PINNACLE GRIPTION 1217-32-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented2 deaths239 reports
- ELEOS™ 25002111EOnkos Surgical, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented3 deaths230 reports
- Novation 130-36-52Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented2 recalls124 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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