Tornier Perform MWE152Recalls & reported problems
Tornier · CANNULATED DRILL/REAMER DRIVER WITH TIP · Class 1
All models of Tornier Perform (10)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 03700386973888), received between Sep 26, 2022 and Sep 27, 2022 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Residue After Decontamination” (2 reports).
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
- Residue After Decontamination2
Patient problems
- Insufficient Information2
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 27, 2022Residue After Decontamination; Residue After Decontamination
IT WAS REPORTED THAT THE TORNIER SURGICAL INSTRUMENT COMPANY REPRESENTATIVE DELIVERED FIVE CANNULATED INSTRUMENTS WITH EXTENSIVE DEBRIS AND RESIDUE INSIDE THE CHANNELS. THE RESIDUE APPEARED TO BE RUST, CHEMICAL RESIDUE, AND POSSIBLE BIOBURDEN. THE INSTRUMENTS WERE LOANER INSTRUMENTS THAT WERE DELIVERED BY THE MILWAUKEE WISCONSIN AREA REPRESENTATIVE FOR TORNIER. THE FIVE INSTRUMENTS, WHICH WERE CANNULATED DRILL/DRIVERS, WERE PART OF THE AEQULAIS PERFORM GLENOID SYSTEM.
Patient problems: Insufficient Information
MAUDE report 15490811 ↗MalfunctionSep 26, 2022Residue After Decontamination; Residue After Decontamination
IT WAS REPORTED THAT THE TORNIER SURGICAL INSTRUMENT COMPANY REPRESENTATIVE DELIVERED FIVE CANNULATED INSTRUMENTS WITH EXTENSIVE DEBRIS AND RESIDUE INSIDE THE CHANNELS. THE RESIDUE APPEARED TO BE RUST, CHEMICAL RESIDUE, AND POSSIBLE BIOBURDEN. THE INSTRUMENTS WERE LOANER INSTRUMENTS THAT WERE DELIVERED BY THE MILWAUKEE WISCONSIN AREA REPRESENTATIVE FOR TORNIER. THE FIVE INSTRUMENTS, WHICH WERE CANNULATED DRILL/DRIVERS, WERE PART OF THE AEQULAIS PERFORM GLENOID SYSTEM.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 15487237 ↗
Other BIT, SURGICAL devices
- Tornier Perform MWJ127Tornier, Inc. · BIT, SURGICAL114 reports
- NA 310.534Synthes GmbH · BIT, SURGICAL64 reports
- NA 4200355042Stryker Corporation · BIT, SURGICAL34 reports
- ACUFEX 72204044Smith & Nephew, Inc. · BIT, SURGICAL25 reports
- NA 03.168.011Synthes GmbH · BIT, SURGICAL20 reports
- ACUFEX 72204042Smith & Nephew, Inc. · BIT, SURGICAL19 reports
- ACUFEX 72204046Smith & Nephew, Inc. · BIT, SURGICAL16 reports
- ACUFEX 72204045Smith & Nephew, Inc. · BIT, SURGICAL14 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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