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Aequalis Reversed II MWF702Recalls & reported problems

Tornier · BIO-RSA Reamer 3-In-1 · Class 1

All models of AEQUALIS REVERSED II (46)

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 03700386977596), received between Mar 30, 2020 and Mar 30, 2020 — classified as 1 injury.

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 18, 2026.

Most reported problems

Device problems

  • Break1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • InjuryMar 30, 2020Break; Break

    THE TORNIER BIO RSA REAMER, WHICH IS USED TO HARVEST A BONE GRAFT FROM THE HUMERAL HEAD, BROKE INTO TWO PIECES WHILE THE GRAFT WAS BEING HARVESTED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 9897201 ↗

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Sources and updates

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