Megasystem C 15-8522/06Recalls & reported problems
WALDEMAR LINK GmbH & Co. KG · Stem Components, Stem Segments · 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 04026575383559), received between Nov 18, 2025 and Nov 18, 2025 — 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
Most reported problems
Device problems
- Fracture1
Patient problems
- Fall1
- Loss of Range of Motion1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 18, 2025Fracture; Fracture
FRACTURE OF THE MALE TAPER OF A STEM SEGMENT [CUSTOMER].
Patient problems: Fall; Loss of Range of Motion
MAUDE report 23579438 ↗
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-1522-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model Replacement Plateau; Item Number: 15-0027/12;
- 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-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-1513-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/02;
- Z-1520-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model Replacement Plateau; Item Number: 15-8521/15;
- 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-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-1515-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model Replacement Plateau; Item Number: 15-2835/12;
- Z-1516-2026 · Jan 12, 2026 · Open, ClassifiedEndo-Model Replacement Plateau; Item Number: 15-2836/11;
- 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-2411-2024 · May 22, 2024 · Open, ClassifiedEndo Model SL Tibial Components 16-2817/02 Tibial Component, Small, W: 60mm 16-2817/05 Tibial Component, Medium, W: 65mm 16-2817/07 Tibial Component, Large, W: 75m
…and 1 more.
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 1115-1217United 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 1115-1213United Orthopedic Corp. · Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer3 recalls0 reports
- Endo-Model Modular Knee Prosthesis System 15-3816/11WALDEMAR LINK GmbH & Co. KG · Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer2 recalls6 reports
- Endo-Model Modular Knee Prosthesis System 15-3816/12WALDEMAR 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 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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