Skip to content

ATTUNE 2546-00-021Recalls & reported problems

Depuy (Ireland) · ATTUNE KNEE SYSTEM REVISION CANAL REAMER 21MM · Class 1

Data updated Oct 13, 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 10603295440109), received between Oct 17, 2018 and Oct 17, 2018 — 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Break1

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.

  • MalfunctionOct 17, 2018Break; Break

    REAMER WAS BROKEN.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7973448 ↗

Other REAMER devices

All REAMER devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page