TORNIER PERFORM™ REVERSED DWJ1017202Recalls & reported problems
Tornier, Inc. · Class 2 · Implant
Data updated Oct 16, 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 00846832085729), received between Aug 31, 2023 and Aug 31, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 16, 2026.
Most reported problems
Device problems
- Device Dislodged or Dislocated1
Patient problems
- Joint Dislocation1
- Osteolysis1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 31, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated
A REVISION SURGERY WAS CONDUCTED USING THE BLUEPRINT PLANNING FEATURE. THE REASON FOR THE REVISION WAS THAT THE PATIENT'S BASEPLATE BECAME DISLODGED FROM THE GLENOID WITHIN TWO WEEKS OF THE INITIAL SURGERY. THE DEVICES REMOVED DURING THE REVISION WERE THE BASEPLATE AND THE GLENOSPHERE. THE INITIAL SURGERY ENCOUNTERED CHALLENGES, INCLUDING A DROP OFF ON THE POSTERIOR GLENOID DUE TO BONE LOSS, WHICH LIKELY CONTRIBUTED TO THE BASEPLATE NOT BEING PROPERLY SECURED. ADDITIONALLY, ONE OF THE PERIPHERAL SCREWS HAD BROKEN DURING THE INITIAL SURGERY, BUT IT WAS NOT DEEMED TO BE THE CAUSE OF THE REVISION.
Patient problems: Joint Dislocation; Osteolysis
MAUDE report 17660107 ↗
Other shoulder prosthesis, reverse configuration devices
- DJO SURGICAL 508-36-101Encore Medical, L.P. · shoulder prosthesis, reverse configuration508 reports
- DJO SURGICAL 508-32-101Encore Medical, L.P. · shoulder prosthesis, reverse configuration433 reports
- DJO SURGICAL 508-32-103Encore Medical, L.P. · shoulder prosthesis, reverse configuration421 reports
- DJO SURGICAL 509-00-036Encore Medical, L.P. · shoulder prosthesis, reverse configuration1 recall259 reports
- DJO SURGICAL 508-32-104Encore Medical, L.P. · shoulder prosthesis, reverse configuration1 recall203 reports
- DJO SURGICAL 509-00-032Encore Medical, L.P. · shoulder prosthesis, reverse configuration233 reports
- DELTA XTEND 130760000Depuy (Ireland) · shoulder prosthesis, reverse configuration223 reports
- DJO SURGICAL 508-00-032Encore Medical, L.P. · shoulder prosthesis, reverse configuration122 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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