SMR TT Augmented 360 1375.15.565Recalls & reported problems
Limacorporate SPA · SMR TT Augmented 360 Baseplate S-R 15°X · 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 08033390180337), received between Mar 12, 2026 and Mar 12, 2026 — 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.
Reports received per month
Most reported problems
Device problems
- Device Dislodged or Dislocated1
- Patient Device Interaction Problem1
Patient problems
- Joint Dislocation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 12, 2026Device Dislodged or Dislocated; Patient Device Interaction Problem
REVISION SURGERY WAS PERFORMED ON (B)(6) 2026, WITH REMOVAL OF THE GLENOID COMPONENT DUE TO LOOSENING AND IMPLANT DISLOCATION. ALL COMPONENTS WERE EXPLANTED, WITH THE EXCEPTION OF THE UNCEMENTED HUMERAL STEM, WHICH REMAINED IMPLANTED. WEAR WAS OBSERVED ON THE GLENOID TT PEG, PROBABLY CAUSED BY SCRAPING FROM THE LATERALIZED INLAY AFTER FAILURE OF GLENOID COMPONENTS. THE PATIENT HAD PREVIOUSLY UNDERGONE SURGERY ON (B)(6) 2025 (OUR COMPLAINT REFERENCE (B)(4)), WHICH WAS THE FIRST REVISION PROCEDURE OF A PRIMARY REVERSE SHOULDER ARTHROPLASTY (RSA) PERFORMED ON (B)(6) 2023, DUE TO LOOSENING OF THE GLENOID COMPONENTS. THE FOLLOWING DEVICES WERE EXPLANTED DURING THE REVISION SURGERY ON (B)(6) 2026: · SMR REVERSE HP GLENOSPH. 40 MM (PRODUCT CODE: 1374.50.400, LOT: 2517230 - STER: (B)(6)) - SOLD IN US. · TT AUGM.360 BASEPLATE S-R 15°X (PRODUCT CODE: 1375.15.565, LOT: 2517898 - STER: (B)(6)) - SOLD IN US · SMR REVERSE HUMERAL BODY SHORT (PRODUCT CODE:1352.15.005, LOT:2422027 - STER: (B)(6)) - SOLD IN US · SMR REV. HP LAT. LINER MEDIUM(PRODUCT CODE:1365.09.115, LOT:2519411 - STER: (B)(6)) - SOLD IN US · SMR CONNECTOR SMALL R (PRODUCT CODE:1374.15.305, LOT: 2523844 - STER: (B)(6)) - SOLD IN US
Patient problems: Joint Dislocation
MAUDE report 24581096 ↗
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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