Tornier Perform MWJ138Recalls & reported problems
Tornier, Inc. · Lateralized Glenosphere Trial · Class 1
All models of Tornier Perform (40)
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 00846832062591), received between Aug 24, 2022 and Aug 24, 2022 — 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 18, 2026.
Most reported problems
Device problems
- Break1
- Fracture1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 24, 2022Break; Fracture; Break; Fracture
IT WAS REPORTED THAT WHILE REMOVING THE TRIAL FROM THE BASEPLATE, THE CENTRAL PLASTIC PORTION THAT SURROUNDS THE SCREW BROKE OFF FROM THE SURROUNDING TRIAL. THE ISSUE WAS NOTICED AS THE SMALL PIECE OF PLASTIC WAS STILL IN THE JOINT, AND WAS NOTICED BY THE SURGEON.
Patient problems: Foreign Body In Patient
MAUDE report 15284393 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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