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SPECIALIST 96-6430Recalls & reported problems

Depuy (Ireland) · SPECIALIST 2 TIBIAL INSERT TRIAL REMOVER · Class 1

All models of SPECIALIST (80)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295248439), received between May 28, 2020 and May 28, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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

  • Break1
  • Naturally Worn1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionMay 28, 2020Break; Naturally Worn; Break; Naturally Worn

    BROKEN LCS HANDLE DUE TO SURGEON DROPPING IT ON THE GROUND. THE ROUND SPACER RING HAS COME OFF THE HANDLE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 10096602 ↗

Other EXTRACTOR devices

All EXTRACTOR devices →

Sources and updates

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