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SPECIALIST 97-6755Recalls & reported problems

Depuy Orthopaedics, Inc. · SPECIALIST 2 PATELLAR PLANER DEPTH GAUGE · Class 1

All models of SPECIALIST (12)

Data updated Oct 18, 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 10603295251538), received between May 12, 2023 and May 12, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Incorrect Measurement” (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

  • Incorrect Measurement1
  • Naturally Worn1

Patient problems

  • Insufficient Information1

Recent adverse event reports

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

  • MalfunctionMay 12, 2023Incorrect Measurement; Naturally Worn; Incorrect Measurement; Naturally Worn

    IT WAS REPORTED THAT THE DEPTH GAUGE NUMBERS ARE COMPLETELY WORN OFF AND DEPTHS AREN¿T EXACTLY ACCURATE.

    Patient problems: Insufficient Information

    MAUDE report 16918198 ↗

Other GAUGE, DEPTH devices

All GAUGE, DEPTH devices →

Sources and updates

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