Endo-Model SL Knee Prosthesis System 16-2817/07Recalls & reported problems
WALDEMAR LINK GmbH & Co. KG · Tibial Component,neutral · Class 2 · Implant
All models of Endo-Model SL Knee Prosthesis System (25)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 2
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
2 FDA recall records name this device's identifier, 2 still open.
15 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.
Recalls naming this device
- May 22, 2024Class IIOpen, Classified
Blind screws of the modular tibial component cannot be loosened intraoperatively,prolongation surgery due to intraoperatively change in procedure, probably to cementing technique
Z-2411-2024 · Root cause: Process design · Recall details · FDA record ↗
- May 24, 2022Class IIOpen, Classified
There is a risk that blind screws of the modular tibial component cannot be loosened intraoperatively. This may lead to prolongation of surgery due to an intraoperative change in procedure.
Z-1379-2022 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
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-1513-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/02;
- Z-1515-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model Replacement Plateau; Item Number: 15-2835/12;
- Z-1518-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model Replacement Plateau; Item Number: 15-8521/09;
- Z-1517-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model Replacement Plateau; Item Number: 15-8030/12;
- Z-1520-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model Replacement Plateau; Item Number: 15-8521/15;
- Z-1519-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model Replacement Plateau; Item Number: 15-8521/11;
- Z-1523-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model Replacement Plateau; Item Number: 15-0027/16;
- Z-1522-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model Replacement Plateau; Item Number: 15-0027/12;
- Z-1516-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model Replacement Plateau; Item Number: 15-2836/11;
- Z-1521-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model Replacement Plateau; Item Number: 15-0027/11;
- Z-1514-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/07;
- Z-1511-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/05;
- Z-1512-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model Replacement Plateau; Item Number: 15-0027/15;
- 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
Other Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer devices
- ELEOS™ 25001208EOnkos Surgical, Inc. · PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER3 deaths193 reports
- ELEOS™ THSMWRS01MOnkos Surgical, Inc. · PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER190 reports
- "UNITED" USTAR II Hip System 1115-1413United Orthopedic Corp. · Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer3 recalls3 reports
- "UNITED" USTAR II Hip System 1115-1213United Orthopedic Corp. · Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer3 recalls0 reports
- "UNITED" USTAR II Hip System 1115-1417United Orthopedic Corp. · Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer3 recalls0 reports
- "UNITED" USTAR II Hip System 1115-1217United Orthopedic Corp. · Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer3 recalls0 reports
- Endo-Model Modular Knee Prosthesis System 15-3816/12WALDEMAR LINK GmbH & Co. KG · Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer2 recalls6 reports
- Endo-Model Modular Knee Prosthesis System 15-3816/11WALDEMAR LINK GmbH & Co. KG · Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer2 recalls6 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
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- 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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