SMR TT Hybrid GlenoidRecalls & reported problems across all models
Limacorporate SPA · 3 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names at least one SMR TT Hybrid Glenoid model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls
- 1
We found 3 models of SMR TT Hybrid Glenoid by Limacorporate SPA in the FDA's device registry (GUDID). Together they are named in 2 adverse event reports in the FDA's MAUDE database, received between Mar 24, 2026 and Jul 1, 2026 — classified as 2 injuries.
1 FDA recall record name at least one of these models by its device identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
SMR TT Hybrid Glenoid recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Feb 21, 2023Class IIOpen, Classified
Shoulder glenoid fossa prosthesis was manufactured without tantalum markers so in the absence of the markers, on already implanted devices, a correct radiographic assessment of the hybrid glenoid position can be performed by the evaluation of the joint space, central TT peg position and cement mantel observation.
Z-1317-2023 · Root cause: Process control · Recall details · FDA record ↗
Most reported SMR TT Hybrid Glenoid problems
Device problems
- Adverse Event Without Identified Device or Use Problem2
Patient problems
- Muscle/Tendon Damage2
SMR TT Hybrid Glenoid models
3 models, most reported first. Each model has its own page with its reports, recalls and device details.
- SMR TT Hybrid Glenoid 1379.59.210Shoulder Prosthesis, Reverse Configuration1 recall0 reports
- SMR TT Hybrid Glenoid 1379.59.100Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented1 report
- SMR TT Hybrid Glenoid 1379.59.110Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented1 report
Recent SMR TT Hybrid Glenoid adverse event reports
The 2 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryJul 1, 2026Adverse Event Without Identified Device or Use Problem
REVISION SURGERY WAS PERFORMED ON (B)(6) 2026 DUE TO CUFF FAILURE. THE PATIENT UNDERWENT A PRIMARY TOTAL SHOULDER ARTHROPLASTY ABOUT 6 YEAR AGO WITH A CATALYST HUMERAL HEAD AND LIMA TT HYBRID GLENOID (PN 1379.59.100). DUE TO CUFF FAILURE, THE PATIENT HAS BEEN CONVERTED TO A REVERSE CONFIGURATION, REMOVING THE PRE-EXISTING GLENOID AND REPLACING IT WITH THE TT HYBRID REVERSE BASEPLATE (PM 1379.15.160) AND 36MM GLENOSPHERE (PN 1374.09.111). NO INFORMATION REGARDING HUMERAL PART WERE PROVIDED. PATIENT IS FEMALE, DATE OF BIRTH (B)(6) 2026. THE EVENT OCCURRED IN THE UNITED STATES.
Patient problems: Muscle/Tendon Damage
MAUDE report 25680178 ↗InjuryMar 24, 2026Adverse Event Without Identified Device or Use Problem
REVISION SURGERY WAS PERFORMED ON (B)(6) 2026, DUE TO CUFF FAILURE. PREVIOUS SURGERY WAS PERFORMED ON (B)(6) 2020. DURING THE REVISION SURGERY THE PRE-EXISTING TT HYBRID CEM. GLENOID SMALL (PN 1379.59.110) HAS BEEN REMOVED AND PROSTHESIS CONVERTED TO REVERSE CONFIGURATION IMPLANTING A NEW SMR TT HYBRID REVERSE BASEPLATE (PN 1379.15.160) AND SMR GLENOSPHERE DIA. 36MM (PN 1374.09.111). NO INFORMATION REGARDING ORIGINAL AND REVISED HUMERAL COMPONENTS WERE PROVIDED. SURGERY WAS COMPLETED AS INTENDED. PATIENT IS FEMALE, DATE OF BIRTH (B)(6) 1954. EVENT OCCURRED IN THE UNITED STATES.
Patient problems: Muscle/Tendon Damage
MAUDE report 24680602 ↗
Other Limacorporate SPA products
All Limacorporate SPA devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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