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NEXGEN® 00-5886-047-12Recalls & reported problems

Zimmer Trabecular Metal Technology Inc. · Class 2 · Implant

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 00889024310179), received between May 6, 2020 and May 6, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Unstable” (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 18, 2026.

Most reported problems

Device problems

  • Unstable1

Patient problems

  • Limited Mobility Of The Implanted Joint1
  • Muscular Rigidity1
  • Pain1

Recent adverse event reports

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

  • InjuryMay 6, 2020Unstable; Unstable

    IT HAS BEEN REPORTED BILATERAL TOTAL KNEE ARTHROPLASTIES PERFORMED APPROXIMATELY TWO YEARS AGO. AT THE ONE YEAR POSTOP VISIT, THE PATIENT REPORTED MODERATE PAIN, STIFFNESS WITH SITTING, AND SOME INSTABILITY IN THE RIGHT KNEE. NO INTERVENTION OR TREATMENT HAS BEEN GIVEN, AND THE PATIENT REMAINS SATISFIED.

    Patient problems: Limited Mobility Of The Implanted Joint; Muscular Rigidity; Pain

    MAUDE report 10029893 ↗

Other PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER devices

All PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER devices →

Sources and updates

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