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NexGen® 5880-40-23Recalls & reported problems

Zimmer, Inc. · Class 2 · Implant

All models of NexGen (198)

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 00889024199347), received between Jun 16, 2020 and Jun 16, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (1 report).

4 other recalls cover devices cleared under the same FDA submission (K013385, K173057); 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.

Most reported problems

Device problems

  • Device Dislodged or Dislocated1

Patient problems

  • Joint Dislocation1

Recent adverse event reports

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

  • InjuryJun 16, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated

    IT WAS REPORTED THAT A PATIENT WAS REVISED APPROXIMATELY THREE YEARS AND TWO WEEKS POST IMPLANTATION DUE TO DISLOCATION. AT DIAGNOSIS IT WAS DISCOVERED THAT THE HINGE POST CAME OFF. THERE IS NO ADDITIONAL INFORMATION AVAILABLE AT THIS TIME.

    Patient problems: Joint Dislocation

    MAUDE report 10158442 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K013385, K173057. One submission often covers many models, so check the product and lot details in each record.

  • Z-2092-2023 · May 19, 2023 · Terminated
    NexGen Precoat Stemmed Tibial Plate Size 5
  • Z-0321-2020 · Oct 10, 2019 · Terminated
    Various Knee Systems for knee joint arthroplasty, knee prosthesis, Item Nos. 00522000100 00522000200 00522000300 00522000400 00522006304 00522006504 00522006600 00522006800 0052200
  • Z-1447-04 · Aug 3, 2004 · Terminated
    Zimmer brand NEXGEN Complete Knee Solution Rotating Hinge Knee Tibial Component, precoat, nonmodular, size 2, sterile, for cemented use only; Cat. No. 5880-02-02.
  • Z-1448-04 · Aug 3, 2004 · Terminated
    Zimmer brand NEXGEN Complete Knee Solution Rotating Hinge Knee Tibial Component, precoat, nonmodular, size 3, sterile, for cemented use only; Cat. No. 5880-03-02.

Other PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER devices

All PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER devices →

Sources and updates

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