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AESCULAP NR292KRecalls & reported problems

Aesculap AG · FEMUR EXTENS.STEM 6° D15X77MM CEMENTED · 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 04046963339890), received between Aug 26, 2021 and Aug 26, 2021 — classified as 1 injury.

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

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.

Most reported problems

Device problems

  • Fracture1

Patient problems

  • Failure of Implant1

Recent adverse event reports

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

  • InjuryAug 26, 2021Fracture; Fracture

    ADDITIONAL INFORMATION RECEIVED: INVOLVED COMPONENT NR871M. REVISION SURGERY : (B)(6) 2021. INVOLVED COMPONENTS NB017K - ENDURO FEMORAL COMPONENT CEMENTED F1R - LOT UNKNOWN. NR871M - ENDURO MENISCAL COMPONENT F1 12MM - LOT 51788770.

    Patient problems: Failure of Implant

    MAUDE report 12374225 ↗

Other PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER devices

All PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER devices →

Sources and updates

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